[生物醫學研究所] 期刊論文 |
2010-03-01 |
Resectoscopic excision of the vaginal septum in a virgin with uterus didelphys and obstructed unilateral vagina |
Chao-Lan Shih; Yao-Ching Hung; Chih-Ping Chen; Shu-Chin Chien; Wu-Chou Lin |
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[生物醫學研究所] 期刊論文 |
2009-09-01 |
Genetic evaluation and management of fetal chylothorax: review and insights from a case of Noonan syndrome |
Chen C-H; Chen T-H; Kuo S-J; Chih-Ping Chen; Lee D-J; Ke Y-Y; Yeh K-T; Ma G-C; Liu C-S; Shih J-C; Chen Ming |
|
[生物醫學研究所] 期刊論文 |
2008-01-01 |
Association of interleukin-18 gene polymorphism with asthma in Chinese patients |
Cheng-Chun Lee; Wei-Yong Lin; Lei Wan; Yuhsin Tsai; Chang-Hai Tsai; Chung-Ming Huang; Chih-Ping Chen; Fuu-Jen Tsai |
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[生物醫學研究所] 期刊論文 |
2011-09-01 |
The use of misoprostol in termination of second-trimester pregnancy |
Chen-Ju Lin; Shu-Chin Chien; Chih-Ping Chen |
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[生物醫學研究所] 期刊論文 |
2011-02-01 |
MUC4 gene polymorphisms associate with endometriosis development and endometriosis-related infertility |
Cherry Yin-Yi Chang; Hui-Wen Chang; Chih-Mei Chen; Chia-Ying Lin; Chih-Ping Chen; Chih-Ho Lai; Wei-Yong Lin; Hsing-Ping Liu; Jim Jinn-Chyuan Sheu; Fuu-Jen Tsai |
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[生物醫學研究所] 期刊論文 |
2007-11-01 |
Molecular assay of -α3.7 and -α4.2 deletions causing α-thalassemia by denaturing high-performance liquid chromatography |
Chia-Cheng Hung; Chien-Nan Lee; Chih-Ping Chen; Yuh-Jyh Jong; Wu-Shiun Hsieh; Win-Li Lin; Yi-Ning Su; Su-Ming Hsu |
|
[生物醫學研究所] 期刊論文 |
2011-05-01 |
Low penetrance of retinoblastoma for p.V654L mutation of the RB1 gene |
Chia-Cheng Hung; Shin-Yu Lin; Chien-Nan Lee; Chih-Ping Chen; Shuan-Pei Lin; Mei-Chyn Chao; Shyh-Shin Chiou; Yi-Ning Su |
|
[生物醫學研究所] 期刊論文 |
2009-11-01 |
Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome |
Chia-Cheng Hung; Shin-Yu Lin; Chien-Nan Lee; Hui-Yu Cheng; Shuan-Pei Lin; Ming-Ren Chen; Chih-Ping Chen; Chien-Hui Chang; Chiou-Ya Lin; Chih-Chieh Yu; Hsin-Hui Chiu,; Wen-Fang Cheng; Hong-Nerng Ho; Dau-Ming Niu; Yi-Ning Su |
|
[生物醫學研究所] 期刊論文 |
2011-11-01 |
Quantitative and qualitative analyses of the SNRPN gene using real-time PCR with melting curve analysis |
Chia-Cheng Hung; Shin-Yu Lin; Shuan-Pei Lin; Chih-Ping Chen; Lang-Yao Chen; Chien-Nan Lee; Yi-Ning Su |
|
[生物醫學研究所] 期刊論文 |
2009-09-01 |
Identification of CpG methylation of the SNRPN gene by methylation-specific multiplex PCR |
Chia-Cheng Hung; Shin-Yu Lin; Shuan-Pei Lin,; Dou-Ming Niu; Ni-Chung Lee; Wen-Fang Cheng; Chih-Ping Chen; Win-Li Lin; Chien-Nan Lee; Yi-Ning Su |
|
[生物醫學研究所] 期刊論文 |
2007-11-01 |
The roles of serum leptin concentration and polymorphism in leptin receptor gene at codon 109 in breast cancer |
Chien-Liang Liu; Yuan-Ching Chang; Shih-Ping Cheng; Schu-Rern Chern; Tsen-Long Yang; Jie-Jen Lee; Ing-Cherng Guo; Chih-Ping Chen |
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[生物醫學研究所] 期刊論文 |
2007-09-01 |
Perinatal imaging findings of Galloway-Mowat syndrome |
Chih-Ping Chen.; Shuan-Pei Lin; Jeng-Daw Tsai; Jon-Kway Huang; Jui-Lung Yen; Ching-Chang Tseng; Wayseen Wang |
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[生物醫學研究所] 期刊論文 |
2009-03-01 |
Placental abnormalities and preeclampsia in trisomy 13 pregnancies |
Chih-Ping Chen.; |
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[生物醫學研究所] 期刊論文 |
2008-03-01 |
Concomitant occurrence of holoprosencephaly and omphalocele |
Chih-Ping Chen.; |
|
[醫學系] 期刊論文 |
2013-06-01 |
Maternal transmission of interstitial microdeletion in 5q13.2 detected during prenatal diagnosis of coarctation of the aorta |
Chih-Ping Chen; Chen-Ju Lin; Chen-Yu Chen; Schu-Rern Chern; Peih-Shan Wu; Jun-Wei Su; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2007-03-01 |
Second-trimester diagnosis of limb-body wall complex with literature review of pathogenesis |
Chih-Ping Chen; Chen-Ju Lin; Tung-Yao Chang; Chin-Yuan Hsu; Chin-Yuan Tzen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2007-03-01 |
Prenatal diagnosis of the hypoplastic right heart syndrome with sex chromosome pentasomy (49,XXXXY) |
Chih-Ping Chen; Chen-Ju Lin; Tung-Yao Chang; Schu-Rern Chern; Chin-Yuan Tzen; Wen-Lin Chen; Wayseen Wang |
|
[醫學系] 期刊論文 |
2013-12-01 |
Female pseudohermaphroditism in a prenatally diagnosed cloacal malformation with hydronephrosis, dilated bladder, hydrometrocolpos, and oligohydramnios |
Chih-Ping Chen; Chen-Yu Chen; Jun-Wei Su; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-12-01 |
First-trimester prenatal diagnosis of Ellis-van Creveld syndrome |
Chih-Ping Chen; Chen-Yu Chen; Schu-Rern Chern; Jun-Wei Su; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2007-05-01 |
Prenatal diagnosis of mosaic ring chromosome 4 |
Chih-Ping Chen; Chin-Yuan Hsu; Chin-Yuan Tzen; Chen-Chi Lee; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2007-01-01 |
Prenatal diagnosis of pentalogy of Cantrell associated with hypoplasia of the right upper limb and ectrodactyly |
Chih-Ping Chen; Chin-Yuan Hsu; Chin-Yuan Tzen; Schu-Rern Chern; Wayseen Wang |
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[生物醫學研究所] 期刊論文 |
2011-12-01 |
Conjoined twins detected in the first trimester: a review |
Chih-Ping Chen; Chin-Yuan Hsu; Jun-Wei Su; Hsiao-En Cindy Chen; Alan Hwa-Ruey Hsieh; Alex Hwa-Jiun Hsieh; Wayseen Wang |
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[生物醫學研究所] 期刊論文 |
2011-12-01 |
Magnetic resonance imaging demonstration of sirenomelia in one fetus of a dizygotic twin pregnancy conceived by intracytoplasmic sperm injection, in vitro fertilization and embryo transfer |
Chih-Ping Chen; Chin-Yuan Hsu; Maw-Shuan Lee; Yu-Peng Liu; Fuu-Jen Tsai; Pei-Chen Wu; Schu-Rern Chern; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-06-01 |
Prenatal ultrasound demonstration of limb-body wall complex with megacystis |
Chih-Ping Chen; Chin-Yuan Hsu; Pei-Chen Wu; Fuu-Jen Tsai; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2008-12-01 |
Concomitant exencepahly and limb defects associated with pentalogy of Cantrell |
Chih-Ping Chen; Chin-Yuan Tzen; Chen-Yu Chen; Fuu-Jen Tsai; Wayseen Wang |
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[生物醫學研究所] 期刊論文 |
2009-01-01 |
A 12 Mb deletion of 6p24.1->pter in an 18-gestational-week fetus with orofacial clefting, the Dandy-Walker malformation and bilateral multicystic kidneys |
Chih-Ping Chen; Chin-Yuan Tzen; Schu-Rern Chern; Fuu-Jen Tsai; Chin-Yuan Hsu; Chen-Chi Lee; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-09-01 |
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21 |
Chih-Ping Chen; Chyi-Chyang Lin; Tsang-Ming Ko; Fuu-Jen Tsai; Schu-Rern Chern; Chen-Chi Lee; Yu-Ting Chen; Pei-Chen Wu; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-09-01 |
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22 |
Chih-Ping Chen; Chyi-Chyang Lin; Yi-Ning Su; Fuu-Jen Tsai; Schu-Rern Chern; Chen-Chi Lee; Wen-Ling Chen; Li-Feng Chen; Pei-Chen Wu; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-06-01 |
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18 |
Chih-Ping Chen; Chyi-Chyang Lin; Yi-Ning Su; Fuu-Jen Tsai; Yu-Ting Chen; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town; Li-Feng Chen; Pei-Chen Wu; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2008-03-01 |
Triploidy and fetal holoprosencephaly |
Chih-Ping Chen; Edison Shieh; Schu-Rern Chern; Wayseen Wang |
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[生物醫學研究所] 期刊論文 |
2011-12-01 |
Prenatal diagnosis of mosaic trisomy 9 |
Chih-Ping Chen; Fang-Yu Hung; Yi-Ning Su; Schu-Rern Chern; Jun-Wei Su; Chen-Chi Lee; Yu-Ting Chen; Wen-Lin Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-09-01 |
Prenatal diagnosis of satellited 21q derived from pericentric inversion involving the satellite stalk region and terminal 21q |
Chih-Ping Chen; Fuu-Jen Tsai; Chen-Chi Lee; Wen-Lin Chen; Chen-Wen Pan; Pei-Chen Wu; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2008-12-01 |
Limb-body wall complex with craniofacial defects after ovarian stimulation |
Chih-Ping Chen; Fuu-Jen Tsai; Chen-Yu Chen; Hung-Hung Lin; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2007-12-01 |
Cytogenetic variability in the proportion of abnormal cells between the various tissues in prenatally detected mosaic tetrasomy 12p |
Chih-Ping Chen; Fuu-Jen Tsai; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town; Wayseen Wang |
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[生物醫學研究所] 期刊論文 |
2009-03-01 |
Prenatal diagnosis of 46,XX,der(13;21)(q10;q10),+21 and transient abnormal myelopoiesis in a fetus with hepatosplenomegaly and spontaneous resolution of fetal ascites |
Chih-Ping Chen; Fuu-Jen Tsai; Schu-Rern Chern; Tung-Yao Chang; Chin-Yuan Hsu; Hung-Hung Lin; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-06-01 |
Partial monosomy 9p (9p22.2->pter) and partial trisomy 18q (18q21.32->qter) in a female infant with anorectal malformations |
Chih-Ping Chen; Hsien-Ming Lin; Cheung Leung; Shuan-Pei Lin; Yi-Ning Su; Jun-Wei Su; Yu-Ting Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-09-01 |
Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses |
Chih-Ping Chen; Hsien-Ming Lin; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-12-01 |
A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings |
Chih-Ping Chen; Hsu-Kuaing Huang; Pei-Ying Lin; Yi-Ning Su; Ming Chen; Fuu-Jen Tsai; Pei-Chen Wu; Schu-Rern Chern; Yu-Ting Chen; Chen-Chi Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-03-01 |
Trisomy 7 mosaicism at amniocentesis: interphase FISH, QF-PCR and aCGH analyses on uncultured amniocytes for rapid distinguishing true mosaicism from pseudomosaicism |
Chih-Ping Chen; Hsu-Kuang Huang; Yi-Ning Su; Schu-Rern Chern; Jun-Wei Su; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Yu-Ting Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-03-01 |
Prenatal ultraousnd and magnetic resonance imaging findings of fetal akinesia deformation sequence with multiple pterygium syndrome |
Chih-Ping Chen; Jin-Chung Shih; Chen-Yu Chen; Yu-Peng Liu; Schu-Rern Chern; Jun-Wei Su; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2008-03-01 |
Prenatal visualization of cebocephaly with a prominent nose in a second-trimester fetus with alobar holoprosencephaly and trisomy 13 |
Chih-Ping Chen; Jin-Chung Shih; Chin-Yuan Tzen; Schu-Rern Chern; Chen-Ju Lin; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-03-01 |
Prenatal ultrasound demonstration of scoliosis, absence of one rib, a radial club hand, congenital heart defects and absent stomach in a fetus with VACTERL association |
Chih-Ping Chen; Jin-Chung Shih; Ming-Chao Huang; Yu-Peng Liu; Jun-Wei Su; Schu-Rern Chern; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-06-01 |
Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis |
Chih-Ping Chen; Jui-Der Liou; Chi-Hsin Chiang,; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Yu-Ting Chen; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-12-01 |
A 20.5-Mb germline deletion of 13q13.1→q14.3 and somatic mutations of the RB1 gene in an 8-year-old girl with unilateral retinoblastoma, developmental delay and mental retardation |
Chih-Ping Chen; Ling-Yuh Kao; Yi-Ning Su; Ming Chen; Shueen-Dyh Chang; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2009-12-01 |
Limb-body wall complex in one fetus of a dizygotic twin pregnancy conceived by egg donation, in vitro fertilization and embryo transfer: prenatal diagnosis and literature review |
Chih-Ping Chen; Maw-Shuan Lee; Fuu-Jen Tsai; Ming-Chao Huang; Schu-Rern Chern; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-06-01 |
Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome |
Chih-Ping Chen; Ming Chen; Gwo-Chin Ma; Shun-Ping Chang; Yi-Yung Chen; Pei-Chen Wu; Li-Feng Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-09-01 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2 |
Chih-Ping Chen; Ming Chen; Schu-Rern Chern; Peih-Shan Wu; Shun-Ping Chang; Dong-Jay Lee; Yu-Ting Chen; Li-Feng Chen; Jun-Wei Su; Alan Hwa-Ruey Hsieh; Alex Hwa-Jiun Hsieh; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-12-01 |
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8 |
Chih-Ping Chen; Ming Chen; Tsang-Ming Ko; Gwo-Chin Ma; Fuu-Jen Tsai; Ming-Song Tsai; Pei-Chen Wu; Chen-Chi Lee; Li-Feng Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-09-01 |
Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review |
Chih-Ping Chen; Ming Chen; Yi-Ju Pan; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Yu-Ting Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-09-01 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly |
Chih-Ping Chen; Ming Chen; Yi-Ning Su; Fuu-Jen Tsai; Schu-Rern Chern; Chin-Yuan Hsu; Pei-Chen Wu; Dai-Dyi Town; Dong-Jay Lee; Gwo-Chin Ma; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-06-01 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4 |
Chih-Ping Chen; Ming Chen; Yi-Ning Su; Fuu-Jen Tsai; Schu-Rern Chern; Pei-Chen Wu; Wen-Lin Chen; Li-Feng Chen; Chen-Wen Pan; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-06-01 |
Inv dup del(10q): Identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements |
Chih-Ping Chen; Ming Chen; Yi-Ning Su; Jian-Pei Huang; Gwo-Chin Ma; Shun-Ping Chang; Schu-Rern Chern; Yu-Ting Chen; Jun-Wei Su; Chen-Chi Lee; Dai-Dyi Town; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-12-01 |
Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings |
Chih-Ping Chen; Ming Chen; Yi-Ning Su,; Chin-Yuan Hsu; Fuu-Jen Tsai; Schu-Rern Chern; Pei-Chen Wu; Chen-Chi Lee; Wayseen Wang |
|
[醫學系] 期刊論文 |
2014-02-01 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistry |
Chih-Ping Chen; Ming Cheng; Chen-Yu Chen; Schu-Rern Chern; Peih-Shan Wu; Shun-Ping Chang; Yu-Ling Kuo; Wen-Lin Chen; Chen-Wen Pan; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-12-01 |
Recurrent distal 16q duplication and terminal 22q deletion: prenatal diagnosis and genetic counseling |
Chih-Ping Chen; Ming-Chao Huang; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Dai-Dyi Town; Chen-Wen Pan; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-12-01 |
Microvillus inclusion disease: prenatal ultrasound findings, molecular diagnosis and genetic counseling of congenital diarrhea |
Chih-Ping Chen; Ming-Chou Chiang; Tzu-Hao Wang; Chuen Hsueh; Shueen-Dyh Chang; Fuu-Jen Tsai; Chao-Ning Wang; Schu-Rern Chern; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-03-01 |
Unbalanced reciprocal translocations at amniocentesis |
Chih-Ping Chen; Pei-Chen Wu; Chen-Ju Lin; Schu-Rern Chern; Fuu-Jen Tsai; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Li-Feng Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-12-01 |
Balanced reciprocal translocations detectred at amniocentesis |
Chih-Ping Chen; Pei-Chen Wu; Chen-Ju Lin; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Li-Feng Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-12-01 |
Detection of mosaic balanced homologous acrocentric rearrangement rea(21q21q) in a woman with repeated pregnancy losses |
Chih-Ping Chen; Pei-Chen Wu; Fuu-Jen Tsai; Li-Feng Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-12-01 |
Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of left wrist and aplasia of left thumb |
Chih-Ping Chen; Schu-Rern Chern; Chen-Yu Chen; Pei-Chen Wu; Li-Feng Chen; Chen-Wen Pan; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-06-01 |
Detection of a balanced homologous acrocentric rearrangement rea(14q14q) and low-grade X-chromosome mosaicism in a couple with repeated pregnancy losses |
Chih-Ping Chen; Schu-Rern Chern; Chia-Hsun Wu; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang |
|
[醫學系] 期刊論文 |
2000-01-01 |
Prenatal diagnosis and genetic analysis of X chromosome polysomy 49,XXXXY |
Chih-Ping Chen; Schu-Rern Chern; Chih-Long Chang; Chen-Chi Lee; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2009-09-01 |
Prenatal diagnosis of partial trisomy 14q (14q31.1->qter) and partial monosomy 5p (5p13.2->pter) associated with polyhydramnios, short limbs, micropenis and brain malformations |
Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Chen-Chi Lee; Li-Feng Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2009-09-01 |
Prenatal diagnosis and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly |
Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Chin-Yuan Hsu; Kevin Ko; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2009-09-01 |
Prenatal diagnosis and molecular analysis of trisomy 13 mosaicism |
Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Hung-Hung Lin; Chen-Wen Pan; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-12-01 |
Prenatal diagnosis of partial monosomy 1q (1q42.3→qter) associated with hydrocephalus and corpus callosum agenesis |
Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Hung-Hung Lin; Pei-Chen Wu; Chen-Chi Lee; Chen-Wen Pan; Wayseen Wang. |
|
[生物醫學研究所] 期刊論文 |
2009-12-01 |
Trisomy 13 mosaicism associated with cyclopia and cystic hygroma |
Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2009-12-01 |
Down syndrome due to unbalanced homologous acrocentric rearrangements and its recurrence in subsequent pregnancies: prenatal diagnosis by amniocentesis |
Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Shu-Shien Chiang; Chen-Chi Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2009-12-01 |
Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis |
Chih-Ping Chen; Schu-Rern Chern; Pei-Chen Wu; Fuu-Jen Tsai,; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Li-Feng Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-03-01 |
Unbalanced and balanced heterologous acrocentric rearrangement involving chromosome 21 at amniocentesis |
Chih-Ping Chen; Schu-Rern Chern; Pei-Chen Wu; Fuu-Jen Tsai,; Chen-Chi Lee; Dai-Dyi Town,; Wen-Lin Chen; Li-Feng Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-06-01 |
Prenatal diagnosis and molecular genetic analysis of short rib-polydactyly syndrome type III (Verma-Naumoff) in a second-trimester fetus with a homozygous splice site mutation in intron 4 in the NEK1 gene |
Chih-Ping Chen; Schu-Rern Chern; Tung-Yao Chang; Yi-Ning Su; Yi-Yung Chen; Jun-Wei Su; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-09-01 |
Monozygotic twins with trisomy 18 of paternal origin: prenatal diagnosis and molecular cytogenetic characterization in a pregnancy with one structurally abnormal living fetus and one intrauterine fetal demise |
Chih-Ping Chen; Schu-Rern Chern; Yi-Yung Chen; Pei-Chen Wu; Dai-Dyi Town; Wen-Lin Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2007-03-01 |
Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome) |
Chih-Ping Chen; Shuan-Pei Lin; Chin-Yuan Tzen; Wuh-Liang Hwu; Schu-Rern Chern; Chih-Kuang Chuang; Shu-Shien Chiang; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-06-01 |
Pure distal 11q deletion without additional genomic imbalances in a female infant with Jacobsen syndrome and a de novo unbalanced reciprocal translocation |
Chih-Ping Chen; Shuan-Pei Lin; Chyong-Hsin Hsu; Schu-Rern Chern; Jun-Wei Su; Yen-Jiun Chen; Chen-Wen Pan; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-03-01 |
Clinical imaging findings in a girl with Hutchinson-Gilford progeria syndrome |
Chih-Ping Chen; Shuan-Pei Lin; Dar-Shong Lin; Yu-Peng Liu; Lee James Hsu; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2008-06-01 |
Transient abnormal myelopoiesis of mosaic trisomy 21 presenting fetoplacental cytogenetic discrepancy, hepatosplenomegaly, oligohydramnios and abnormal hematological findings |
Chih-Ping Chen; Shuan-Pei Lin; Fuu-Jen Tsai; Hung-Hung Lin; Schu-Rern Chern; Chih-Kuang Chuang; Chen-Chi Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2008-07-01 |
A 5.6-Mb deletion in 15q14 in a boy with speech and language disorder, cleft palate, epilepsy, a ventricular septal defect, mental retardation and developmental delay |
Chih-Ping Chen; Shuan-Pei Lin; Fuu-Jen Tsai; Schu-Rern Chern; Chen-Chi Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-03-01 |
Congenital tracheal stenosis in a boy with the 22q13.3 deletion syndrome |
Chih-Ping Chen; Shuan-Pei Lin; Fuu-Jen Tsai; Schu-Rern Chern; Pei-Chen Wu; Chen-Chi Lee; Meng-Shan Lee; Yu-Ting Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2008-06-01 |
Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation |
Chih-Ping Chen; Shuan-Pei Lin; Fuu-Jen Tsai; Schu-Rern Chern; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2008-10-01 |
Characterization of a de novo unbalanced Y;autosome translocation in a 45,X mentally retarded male and literature review |
Chih-Ping Chen; Shuan-Pei Lin; Fuu-Jen Tsai; Tzu-Hao Wang; Schu-Rern Chern; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-06-01 |
A de novo supernumerary marker chromosome derived from chromosome 9p (9p13.1->p23) associated with attention deficit and hyperactivity disorder |
Chih-Ping Chen; Shuan-Pei Lin; Jun-Wei Su; Dai-Dyi Town; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-06-01 |
Phenotypic features associated with mosaic tetrasomy 9p in a 20-year-old female patient include autism spectrum disorder |
Chih-Ping Chen; Shuan-Pei Lin; Jun-Wei Su; Meng-Shan Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-09-01 |
Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy, facial asymmetry, psychomotor retardation, kyphoscoliosis, dermatofibrosarcoma and multiple exostoses |
Chih-Ping Chen; Shuan-Pei Lin; Ming Chen; Yi-Ning Su; Schu-Rern Chern,; Tao-Yeuan Wang; Yu-Peng Liu; Fuu-Jen Tsai; Chen-Chi Lee; Yen-Jiun Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-06-01 |
Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactyly |
Chih-Ping Chen; Shuan-Pei Lin; Ming-Ren Chen; Jun-Wei Su; Schu-Rern Chern; Yen-Jiun Chen; Meng-Shan Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-09-01 |
Partial monosomy 3p (3p26.2->pter) and partial trisomy 5q (5q34->qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delay |
Chih-Ping Chen; Shuan-Pei Lin; Ming-Ren Chen; Yi-Ning Su; Schu-Rern Chern; Yu-Peng Liu; Jun-Wei Su; Meng-Shan Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-12-01 |
Pure interstitial duplication of chromosome 7q (7q31.2→q33) in a 4-year-old girl with growth restriction, short stature, speech delay and mental retardation |
Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Fuu-Jen Tsai; Meng-Shan Lee; Yen-Jiun Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-06-01 |
Deletion 2q37.3→qter and duplication 15q24.3→qter characterized by array CGH in a girl with epilepsy and dysmorphic features |
Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Li-Feng Chen; Meng-Shan Lee; Wayseen Wang. |
|
[生物醫學研究所] 期刊論文 |
2010-09-01 |
A de novo 7.9 Mb deletion in 22q13.2→qter in a boy with autistic features, epilepsy, developmental delay atopic dermatitis and abnormal immunological findings |
Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-02-01 |
Prenatal diagnosis of X-linked myotubular myopathy |
Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Fuu-Jen Tsai; Tao-Yeuan Wang; Hung-Hung Lin; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-12-01 |
A 5.3-Mb duplication of 9p12→p13.1 characterized by array CGH in a female infant with developmental delay |
Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Fuu-Jen Tsai,; Chen-Chi Lee; Chen-Wen Pan; Pei-Chen Wu; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-11-01 |
A de novo 4.4-Mb microdeletion in 2p24.3->p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndrome |
Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Peih-Shan Wu; Shuenn-Dyh Chang; Shu-Hang Ng; Yu-Peng Liu; Jun-Wei Su; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-07-01 |
Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2→q24.3 in a girl with autistic features and developmental delay |
Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Yann-Jang Chen; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2007-12-01 |
Abnormal prenatal hematological findings in congenital leukemia of Down syndrome with hepatosplenomegaly |
Chih-Ping Chen; Shuan-Pei Lin; Tung-Yao Chang; Hsin-Tsung Ho |
|
[生物醫學研究所] 期刊論文 |
2007-09-01 |
Prenatal sonographic findings of Klippel-Trénaunay-Weber syndrome |
Chih-Ping Chen; Shuan-Pei Lin; Tung-Yao Chang; Hung-Chang Lee; Han-Yang Hung; Hsiang-Yu Lin; Jian-Pei Huang; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-06-01 |
Apert syndrome associated with upper airway obstruction and gastroesophageal reflux including polyhydramnios in the third trimester |
Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Chen-Yu Chen; Fuu-Jen Tsai; Yu-Peng Liu; Schu-Rern Chern; Pei-Chen Wu; Hsaio-En Cindy Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-03-01 |
Rapid aneuploidy diagnosis of partial trisomy 7q (7q34->qter) and partial monosomy 10q (10q26.12->qter) by array comparative genomic hybridization using uncultured amniocytes |
Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Dai-Dyi Town; Li-Feng Chen; Meng-Shan Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-06-01 |
Uncomplicated vaginal delivery in two consecutive pregnancies carried to term in a woman with osteogenesis imperfecta type I and bisphosphonate treatment before conception |
Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Jian-Pei Huang; Schu-Rern Chern; Jun-Wei Su; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-06-01 |
Pure distal 9p deletion in a female infant with cerebral palsy |
Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Jun-Wei Su; Schu-Rern Chern; Dai-Dyi Town; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-09-01 |
A 24.2-Mb deletion of 4q12→q21.21 characterized by array CGH in a 13½-year-old girl with short stature, mental retardation, developmental delay, hyperopia, exotropia, enamel defects, delayed tooth eruption and delayed puberty |
Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Li-Feng Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-09-01 |
Self-injurious behavior associated with trisomy 9p (9p13.1→p24.3) |
Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Wen-Lin Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-12-01 |
Partial trisomy 1q (1q42.13->qter) and partial monosomy 6q (6q27->qter) in a girl with single median maxillary central incisor, dysgenesis of corpus callosum and developmental delay |
Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Schu-Rern Chern; Jun-Wei Su; Chen-Chi Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-09-01 |
Identification of a missense mutation of c.3064G>A, Gly1022Ser in exon 43 of COL1A1 gene in a girl with osteogenesis imperfecta type III |
Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Schu-Rern Chern; Jun-Wei Su; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-06-01 |
Osteogenesis imperfecta type IV: prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcome |
Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Schu-Rern Chern; Ming-Huei Lin; Jun-Wei Su; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2008-06-01 |
Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutation |
Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Shu-Chin Chien; Fuu-Jen Tsai; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-09-01 |
Mosaic ring chromosome 4 in a child with mild dysmorphisms, congenital heart defects and developmental delay |
Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-12-01 |
De novo satellited 2q associated with corpus callosum dysgenesis, short stature, mental retardation and developmental delay |
Chih-Ping Chen; Shuan-Pei Lin; Yuan-Ling Huang; Schu-Rern Chern; Yu-Peng Liu; Jun-Wei Su; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-06-01 |
Galloway-Mowat syndrome: prenatal ultrasound and perinatal magnetic resonance imaging findings |
Chih-Ping Chen; Shuan-Pei Lin; Yu-Peng Liu; Jeng-Daw Tsai; Chen-Yu Chen; Shin-Lin Shih,; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2007-09-01 |
Prenatal diagnosis of Dandy-Walker malformation associated with distal limb deficiencies |
Chih-Ping Chen; Shu-Chin Chien; Schu-Rern Chern; Chin-Yuan Tzen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-09-01 |
Rapid positive confirmation of trisomy 21 mosaicism at amniocentesis by interphase FISH, QF-PCR and aCGH on uncultured amniocytes |
Chih-Ping Chen; Shuenn-Dyh Chang; Ho-Yen Chueh; Yi-Ning Su; Jun-Wei Su; Schu-Rern Chern; Yu-Ting Chen; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Li-Feng Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-09-01 |
Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase FISH, QF-PCR and aCGH on uncultured amniocytes in a pregnancy with fetal pyelectasis |
Chih-Ping Chen; Shuenn-Dyh Chang; Yi-Ning Su; Ming Chen; Schu-Rern Chern; Jun-Wei Su; Yu-Ting Chen; Wen-Lin Chen; Chen-Wen Pan; Meng-Shan Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-12-01 |
Mosaic isochromosome 20q detected at amniocentesis may be a cell culture artifact |
Chih-Ping Chen; Shuenn-Dyh Chang; Yu-Ting Chen; Jun-Wei Su; Dai-Dyi Town; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-03-01 |
Pathological characterization of a malformed umbilical cord associated with body stalk anomaly |
Chih-Ping Chen; Tao-Yeuan Wang; Pei-Chen Wu; Fuu-Jen Tsai; Wayseen Wang |
|
[醫學系] 期刊論文 |
2014-12-01 |
First-trimester molecular diagnosis of complete hydatidiform mole associated with dizygotic twin pregnancy conceived by intrauterine insemination |
Chih-Ping Chen; Tsang-Ming Ko; Chen-Yu Chen; Tao-Yeuan Wang; Schu-Rern Chern; Yu-Ling Kuo; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-03-01 |
Prenatal diagnosis of partial trisomy 16p (16p12.2->pter) and partial monosomy 22q (22q13.31->qter) associated with increased nuchal translucency and abnormal maternal serum biochemistry in the first trimester |
Chih-Ping Chen; Tsang-Ming Ko; Yi-Ning Su; Chin-Yuan Hsu; Yi-Yung Chen; Jun-Wei Su; Wen-Lin Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-12-01 |
Prenatal diagnosis of mosaic tetrasomy 18p |
Chih-Ping Chen; Tsang-Ming Ko; Yi-Ning Su; Schu-Rern Chern; Jun-Wei Su; Yu-Ting Chen; Dai-Dyi Town; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-12-01 |
Alobar holoprosencephaly, cebocephaly, and micropenis in a Klinefelter fetus of a diabetic mother |
Chih-Ping Chen; Tsung-Hsien Su; Schu-Rern Chern; Jun-Wei Su; Chen-Chi Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-04-01 |
Persistent cloaca presenting with a perineal cyst: prenatal ultrasound and magnetic resonance imaging findings |
Chih-Ping Chen; Tung-Yao Chang; Chin-Yuan Hsu; Yu-Peng Liu; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang |
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[生物醫學研究所] 期刊論文 |
2008-03-01 |
Concomitant omphalocele and anencephaly associated with trisomy 18 and arthrogryposis diagnosed in early pregnancy |
Chih-Ping Chen; Tung-Yao Chang; Hung-Hung Lin; Schu-Rern Chern; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2008-03-01 |
Prenatal sonographic and magnetic resonance imaging demonstration of a right midline arachnoid cyst associated with ventriculomegaly, colpocephaly, dilation of the third ventricle, absence of cavum septi pellucidi, agenesis of the corpus callosum and mega cisterna magna |
Chih-Ping Chen; Tung-Yao Chang; Jeng-Hsiu Hung; Chen-Yu Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2007-04-01 |
Early second-trimester diagnosis of fetal otocephaly |
Chih-Ping Chen; Tung-Yao Chang; Jon-Kway Huang; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2007-04-01 |
Prenatal diagnosis of low-level mosaic tetrasomy 9p by amniocentesis |
Chih-Ping Chen; Tung-Yao Chang; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town; Meng-Shan Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2007-09-01 |
Third-trimester 3D ultrasound evaluation of thanatophoric dysplasia type I |
Chih-Ping Chen; Tung-Yao Chang; Schu-Rern Chern; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-03-01 |
Short rib-polydactyly syndrome type II (Majewski): prenatal diagnosis, perinatal imaging findings and molecular genetic analysis |
Chih-Ping Chen; Tung-Yao Chang; Tao-Yeuan Wang; Chen-Yu Chen; Fuu-Jen Tsai; Pei-Chen Wu; Schu-Rern Chern; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2007-12-01 |
Third-trimester ultrasound evaluation of arachnoid cysts |
Chih-Ping Chen; Tung-Yao Chang; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2008-06-01 |
Prenatal 3-dimensional sonographic and MRI findings in omphalocele-exstrophy-imperforate anus-spinal defects complex |
Chih-Ping Chen; Tung-Yao Chang; Yu-Peng Liu; Fuu-Jen Tsai; Shu-Chin Chien; Chien-Ming Tsao; Hsiao-Bai Yang; Wayseen Wang. |
|
[生物醫學研究所] 期刊論文 |
2007-09-01 |
Prenatal magnetic resonance imaging evaluation of a digynic triploid fetus |
Chih-Ping Chen; Tung-Yao Chang; Yu-Peng Liu; Schu-Rern Chern; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2008-10-01 |
Prenatal diagnosis of partial trisomy 3p (3p21->pter) and partial monosomy 11q (11q23->qter) associated with abnormal sonographic findings of holoprosencephaly, orofacial clefts, pyelectasis and a unilateral duplex renal system |
Chih-Ping Chen; Tzu-Hao Wang; Chyi-Chyang Lin; Fuu-Jen Tsai; Lie-Jiau Hsieh; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2007-10-01 |
Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1 |
Chih-Ping Chen; Tzu-Hao Wang; Yann-Jang Chen; Tung-Yao Chang; Yu-Peng Liu; Chin-Yuan Tzen; Schu-Rern Chern; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2008-04-01 |
NFkB2 gene duplication is associated with fetal pyelectasis in partial trisomy 10q (10q24.1→qter) |
Chih-Ping Chen; Yann-Jang Chen; Fuu-Jen Tsai; Schu-Rern Chern; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2008-09-01 |
Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele |
Chih-Ping Chen; Yann-Jang Chen; Schu-Rern Chern; Fuu-Jen Tsai; Hung-Hung Lin; Chen-Chi Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2008-05-01 |
Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1->er) and partial trisomy 10q (10q25.1->er) |
Chih-Ping Chen; Yann-Jang Chen; Schu-Rern Chern; Fuu-Jen Tsai; Tung-Yao Chang; Chen-Chi Lee; Dai-Dyi Town; Meng-Shan Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-06-01 |
Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10) del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly |
Chih-Ping Chen; Yau-Kun Kuo; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Yu-Ting Chen; Dai-Dyi Town; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-09-01 |
Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization and perinatal findings in a fetus with dup(15)(q26.2q26.3) |
Chih-Ping Chen; Yi-Hui Lin; Heng-Kien Au; Chin-Yuan Hsu; Yu-Peng Liu; Pei-Chen Wu; Schu-Rern Chern; Yu-Ting Chen; Li-Feng Chen; Adam Hwa-Ming Hsieh; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-03-01 |
Mosaic ring chromosome 21, monosomy 21 and isodicentric ring chromosome 21: prenatal diagnosis, molecular cytogenetic characterization and association with 2-Mb deletion of 21q21.1-q21.2 and 5-Mb deletion of 21q22.3 |
Chih-Ping Chen; Yi-Hui Lin; Szu-Yuan Chou; Yi-Ning Su; Schu-Rern Chern; Yu-Ting Chen; Dai-Dyi Town; Wen-Lin Chen; Chen-Wen Pan; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-09-01 |
Pure partial monosomy 3p (3p25.3->pter): prenatal diagnosis and array comparative genomic hybridization characterization |
Chih-Ping Chen; Yi-Ning Su; Chen-Yu Chen; Jun-Wei Su; Schu-Rern Chern; Dai-Dyi Town; Wayseen Wang |
|
[醫學系] 期刊論文 |
2013-10-01 |
Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review |
Chih-Ping Chen; Yi-Ning Su; Chen-Yu Chen; Schu-Rern Chern; Peih-Shan Wu; Jun-Wei Su; Chen-Chi Lee; Li-Feng Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-03-01 |
Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification using uncultured amniocytes in pregnancy with major fetal structural abnormalities |
Chih-Ping Chen; Yi-Ning Su; Chih-Long Chang; Yi-Yung Chen; Jun-Wei Su; Schu-Rern Chern; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-03-01 |
Abnormally flat facial profile on two- and three-dimensional ultrasound and array comparative genomic hybridization for the diagnosis of Pallister-Killian syndrome |
Chih-Ping Chen; Yi-Ning Su; Chin-Yuan Hsu; Fuu-Jen Tsai; Shu-Chin Chien; Schu-Rern Chern; Meng-Shan Lee; Pei-Chen Wu; Hsiao-En Cindy Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-03-01 |
Second-trimester molecular prenatal diagnosis of sporadic Apert syndrome following sonographic findings of mild ventriculomegaly and clenched hands mimicking trisomy 18 |
Chih-Ping Chen; Yi-Ning Su; Chin-Yuan Hsu; Pei-Ying Ling; Fuu-Jen Tsai; Schu-Rern Chern; Pei-Chen Wu; Hsaio-En Cindy Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-12-01 |
Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy |
Chih-Ping Chen; Yi-Ning Su; Chin-Yuan Hsu; Schu-Rern Chern; Chen-Chi Lee; Yu-Ting Chen; Wen-Lin Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-12-01 |
Ellis-van Creveld syndrome: prenatal diagnosis, molecular analysis and genetic counseling |
Chih-Ping Chen; Yi-Ning Su; Chin-Yuan Hsu; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Po-Tsang Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-12-01 |
Prenatal diagnosis of a de novo 17p13.1 microduplication in a fetus with ventriculomegaly and lissencephaly |
Chih-Ping Chen; Yi-Ning Su; Chin-Yuan Hsu; Yu-Peng Liu; Schu-Rern Chern; Li-Feng Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2007-12-01 |
Genetic counseling of prenatally detected unbalanced t(Y;15)(q12;p13) |
Chih-Ping Chen; Yi-Ning Su; Chyi-Chyang Lin; Yueh-Chun Li; Lie-Jiau Hsieh; Chen-Chi Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-06-01 |
Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II |
Chih-Ping Chen; Yi-Ning Su; Fang-Yu Hung; Schu-Rern Chern; Jun-Wei Su; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2009-12-01 |
Terminal 2q deletion and distal 15q duplication: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes |
Chih-Ping Chen; Yi-Ning Su; Fuu-Jen Tsai; Hung-Hung Lin; Schu-Rern Chern; Meng-Shan Lee; Jonathan Kwei Hwang; Teresa Hsiao-Tien Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-06-01 |
Partial monosomy 13q (13q21.32→qter) and partial trisomy 8p (8p12→pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization |
Chih-Ping Chen; Yi-Ning Su; Fuu-Jen Tsai; Ming-Huei Lin; Pei-Chen Wu; Schu-Rern Chern; Chen-Chi Lee; Chen-Wen Pan; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-03-01 |
Rapid genome-wide aneuploidy diagnosis using uncultured amniocytes and array comparative genomic hybridization in pregnancy with abnormal ultrasound findings detected in late second and third trimesters |
Chih-Ping Chen; Yi-Ning Su; Fuu-Jen Tsai; Schu-Rern Chern; Chin-Yuan Hsu; Ming-Chao Huang; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-12-01 |
Partial trisomy 10q (10q25.1→qter) and partial monosomy 13q (13q34→qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization |
Chih-Ping Chen; Yi-Ning Su; Fuu-Jen Tsai; Schu-Rern Chern; Chin-Yuan Hsu; Pei-Chen Wu; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-09-01 |
De novo duplication Xq22.1→q24 with a disruption of the NXF gene cluster in a mentally retarded woman with short stature and premature ovarian failure |
Chih-Ping Chen; Yi-Ning Su; Hung-Hung Lin; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-06-01 |
Fetal magnetic resonance imaging demonstration of central nervous system abnormalities and polydactyly associated with Joubert syndrome |
Chih-Ping Chen; Yi-Ning Su; Jon-Kway Huang; Yu-Peng Liu; Fuu-Jen Tsai; Chun-Kuang Yang; Jian-Pei Huang; Chen-Yu Chen; Pei-Chen Wu; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-03-01 |
Unexplained shortening of the long bones in the third trimester as the only prenatal feature in a male fetus with 45,X/46,X,r(Y) mosaicism |
Chih-Ping Chen; Yi-Ning Su; Ming Chen; Fuu-Jen Tsai; Yi-Yung Chen; Gwo-Chin Ma; Shun-Ping Chang; Jun-Wei Su; Yu-Ting Chen; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-09-01 |
Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation |
Chih-Ping Chen; Yi-Ning Su; Ming Chen; Jian-Pei Huang; Fuu-Jen Tsai; Pei-Chen Wu; Wen-Lin Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-12-01 |
Partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31→qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization |
Chih-Ping Chen; Yi-Ning Su; Richard Shih-Hung Young; Fuu-Jen Tsai; Pei-Chen Wu; Schu-Rern Chern; Dai-Dyi Town; Chen-Wen Pan; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-03-01 |
Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization |
Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Chin-Yuan Hsu; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Meng-Shan Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-03-01 |
Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21→q11.23 by array comparative genomic hybridization |
Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Chin-Yuan Hsu; Chen-Chi Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-06-01 |
Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo interstitial deletion of chromosome 20p |
Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-06-01 |
Mosaic tetrasomy 12p with discrepancy between fetal tissues and extraembryonic tissues: molecular analysis and possible mechanism of formation |
Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Hsaio-En Cindy Chen; Shu-Shien Chiang; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-09-01 |
Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo X;Y translocation |
Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Jun-Wei Su; Yu-Ting Chen; Chen-Chi Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-09-01 |
Prenatal diagnosis of microvillus inclusion disease |
Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Pei-Chen Wu; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-12-01 |
Prenatal diagnosis of an interstitial deletion of 10q (10q11.21->q21.1): array comparative genomic hybridization characterization and literature review |
Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Peih-Shan Wu; Jun-Wei Su; Dai-Dyi Town; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-06-01 |
Detection and comparison of the cytomegalovirus DNA levels in amniotic fluid and fetal ascites in a second-trimester fetus with massive ascites, hyperechogenic bowel, ventriculomegaly and intrauterine growth restriction |
Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Tao-Yeuan Wang; Fuu-Jen Tsai; Hung-Hung Lin; Pei-Chen Wu; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-09-01 |
Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses |
Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Yu-Ming Hwu; Shuan-Pei Lin; Chyong-Hsin Hsu; Fuu-Jen Tsai; Tao-Yeuan Wang; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Li-Feng Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-12-01 |
Prenatal diagnosis of trisomy 8 mosaicism |
Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Yu-Ting Chen; Jun-Wei Su; Chen-Wen Pan; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-12-01 |
Mosaic trisomy 2 at amniocentesis: prenatal diagnosis and molecular genetic analysis |
Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Yu-Ting Chen; Peih-Shan Wu; Jun-Wei Su; Chen-Wen Pan; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-03-01 |
Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations |
Chih-Ping Chen; Yi-Ning Su; Shin-Yu Lin; Chih-Long Chang; Yeou-Lih Wang; Jiau-Pei Huang; Chen-Yu Chen; Fang-Yu Hung; Yi-Yung Chen; Pei-Chen Wu; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-09-01 |
Prenatal diagnosis of mosaic trisomy 2: discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction |
Chih-Ping Chen; Yi-Ning Su; Shin-Yu Lin; Schu-Rern Chern; Yu-Ting Chen; Meng-Shan Lee; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-09-01 |
Rapid aneuploidy diagnosis of trisomy 18 by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal arachnoid cyst detected in late second trimester |
Chih-Ping Chen; Yi-Ning Su; Shun-Long Weng; Fuu-Jen Tsai; Chen-Yu Chen; Yu-Peng Liu; Schu-Rern Chern; Wen-Lin Chen; Pei-Chen Wu; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-06-01 |
Osteogenesis imperfecta type II: prenatal diagnosis and association with increased nuchal translucency and hypoechogenicity of the cranium |
Chih-Ping Chen; Yi-Ning Su; Tung-Yao Chang; Ming-Chao Huang; Chun-Heng Pan; Schu-Rern Chern; Jun-Wei Su; Wayseen Wang |
|
[醫學系] 期刊論文 |
2013-06-01 |
Rapid detection of de novo P253R mutation in FGFR2 using uncultured amniocytes in a pregnancy affected by polyhydramnios, Blake's pouch cyst, and Apert syndrome |
Chih-Ping Chen; Yi-Ning Su; Tung-Yao Chang; Schu-Rern Chern; Chen-Yu Chen; Jun-Wei Su; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-06-01 |
Osteogenesis imperfecta type I: second-trimester diagnosis and incidental identification of a dominant COL1A1 deletion mutation in the asymptomatic father |
Chih-Ping Chen; Yi-Ning Su; Tung-Yao Chang; Schu-Rern Chern; Chen-Yu Chen; Jun-Wei Su; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2009-12-01 |
22q 11.2 microdeletion in a fetus with double-outlet right ventricle, pulmonary stenosis and a ventricular septal defect: prenatal diagnosis by array comparative genomic hybridization |
Chih-Ping Chen; Yi-Ning Su; Tung-Yao Chang; Schu-Rern Chern; Fuu-Jen Tsai; Jonathan Kwei Hwang; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2012-06-01 |
Identification of a deletion mutation in the short flanking repeat region of exon 44 of COL1A1 gene in a fetus with osteogenesis imperfecta type II |
Chih-Ping Chen; Yi-Ning Su; Tung-Yao Chang; Schu-Rern Chern; Jun-Wei Su; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2009-09-01 |
Prenatal magnetic resonance imaging, ultrasound imaging findings and genetic analysis of concomitant rhabdomyomas and cerebral tuberous sclerosis |
Chih-Ping Chen; Yi-Ning Su; Tung-Yao Chang; Yu-Peng Liu; Fuu-Jen Tsai; Jonathan Kwei Hwang; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-09-01 |
Prenatal diagnosis of rhabdomyomas and cerebral tuberous sclerosis by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy associated with a frameshift mutation in the TSC2 gene |
Chih-Ping Chen; Yi-Ning Su; Tung-Yao Chang; Yu-Peng Liu; Fuu-Jen Tsai; Ming-Ren Chen; Jonathan Kwei Hwang; Teresa Hsiao-Tien Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-12-01 |
Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion |
Chih-Ping Chen; Yi-Ning Su; Yi-Yung Chen; Jun-Wei Su; Schu-Rern Chern; Yu-Ting Chen; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang. |
|
[生物醫學研究所] 期刊論文 |
2012-09-01 |
Usefulness of interphase FISH on uncultured amniocytes for rapid confirmation of low-level trisomy 7 mosaicism in a pregnancy with fetal intrauterine growth restriction and microcephaly |
Chih-Ping Chen; Yi-Ning Su; Yi-Yung Chen; Schu-Rern Chern; Jun-Wei Su; Yu-Ting Chen; Dai-Dyi Town; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-09-01 |
Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia and intrauterine growth restriction |
Chih-Ping Chen; Yi-Ning Su; Yi-Yung Chen; Schu-Rern Chern; Yu-Peng Liu; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-09-01 |
Prenatal diagnosis of directly transmitted benign 4q12-q13.1 quadruplication associated with tandem segmental amplifications of the LPHN3 gene |
Chih-Ping Chen; Yi-Ning Su; Yu-Ting Chen; Wen-Lin Chen; Lee James Hsu; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2011-12-01 |
First trimester two-dimensional and three-dimensional ultrasound demonstration of craniofacial defects, abdominal wall defects and upper limb deficiency associated with limb-body wall complex |
Chih-Ping Chen; Yi-Yung Chen; Jun-Wei Su; Wayseen Wang |
|
[醫學系] 期刊論文 |
2002-01-01 |
Bilateral calcified ovarian fibromas in a patient with Sotos syndrome |
Chih-Ping Chen; Yuh-Cheng Yang; Shuan-Pei Lin; Wayseen Wang; Chih-Long Chang; Kuo-Ming Chang |
|
[醫學系] 期刊論文 |
2013-12-01 |
Concordant myelomeningocele in dizygotic twins conceived by intracytoplasmic sperm injection, in vitro fertilization, and embryo transfer |
Chih-Ping Chen; Yuh-Ming Hwu; Chen-Yu Chen; Yi-Ning Su; Tzu-Hung Lin; Yu-Ling Kuo; Schu-Rern Chern; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2008-03-01 |
Occipital encephalocele associated with iniencephaly mimicking an unilateral nuchal tumor on prenatal ultrasound |
Chih-Ping Chen; Yuh-Ming Hwu; Fuu-Jen Tsai; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-09-01 |
Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and dsomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization |
Chih-Ping Chen; Yung-Ting Guo; Shuan-Pei Lin; Yi-Ning Su; Yann-Jang Chen; Rui-Yuan Hseuh; Yi-Hui Lin; Pei-Chen Wu; Chen-Chi Lee,; Yu-Ting Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2009-09-01 |
Concomitant craniorachischisis and omphalocele in a male fetus: prenatal magnetic resonance imaging findings and literature review |
Chih-Ping Chen; Yu-Peng Liu; Fuu-Jen Tsai; Chen-Yu Chen; Hung-Hung Lin; Pei-Chen Wu; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2008-03-01 |
Prenatal evaluation with magnetic resonance imaging of a giant blind ectopic ureter associated with a duplex kidney |
Chih-Ping Chen; Yu-Peng Liu; Jian-Pei Huang; Tung-Yao Chang; Fuu-Jen Tsai; Jeng-DauTsai; Jin-Cherng Sheu; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-03-01 |
Ventriculomegaly, intrauterine growth restriction and congenital heart defects as salient prenatal sonographic findings of Miller-Dieker lissencephaly syndrome associated with monosomy 17p (17p13.2pter) in a fetus |
Chih-Ping Chen; Yu-Peng Liu; Shuan-Pei Lin,; Ming Chen; Fuu-Jen Tsai; Yu-Ting Chen; Li-Feng Chen; Jonathan Kwei Hwang; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2007-03-01 |
Prenatal diagnosis of concomitant gallbladder hydrops and pyelectasis with spontaneous resolution |
Chih-Ping Chen; Yu-Peng Liu; Shu-Chin Chien; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-09-01 |
Prenatal diagnosis of persistent cloaca with hydrometrocolpos and ascites by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy |
Chih-Ping Chen; Yu-Peng Liu; Tung-Yao Chang; Fuu-Jen Tsai; Chen-Yu Chen; Pei-Chen Wu; Teresa Hsiao-Tien Chen; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2007-11-01 |
Ruptured omphalocele with extracorporeal intestines mimicking gastroschisis in a fetus with Turner syndrome |
Chih-Ping Chen,; |
|
[生物醫學研究所] 期刊論文 |
2007-03-01 |
Meckel syndrome: genetics, perinatal findings, and differential diagnosis |
Chih-Ping Chen,; |
|
[生物醫學研究所] 期刊論文 |
2012-03-01 |
Prenatal diagnosis and genetic analysis of fetal akinesia deformation sequence and multiple pterygium syndrome associated with neuromuscular junction disorders: a review |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2010-06-01 |
Pathophysiology of increased fetal nuchal translucency thickness |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2010-03-01 |
Prenatal diagnosis and genetic counseling for mosaic trisomy 13 |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2010-03-01 |
Prenatal sonographic features of fetuses in trisomy 13 pregnancies (IV) |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2009-12-01 |
Prenatal sonographic features of fetuses in trisomy 13 pregnancies (III) |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2009-06-01 |
Prenatal sonographic features of fetuses in trisomy 13 pregnancies (I) |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2009-06-01 |
Prenatal sonographic features of fetuses in trisomy 13 pregnancies (II) |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2008-09-01 |
Prenatal diagnosis, fetal surgery, recurrence risk and differential diagnosis of neural tube defects |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2008-09-01 |
Syndromes, disorders and maternal risk factors associated with neural tube defects (V) |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2008-09-01 |
Syndromes, disorders and maternal risk factors associated with neural tube defects (VI) |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2008-09-01 |
Syndromes, disorders and maternal risk factors associated with neural tube defects (VII) |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2008-06-01 |
Syndromes, disorders and maternal risk factors associated with neural tube defects (III) |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2008-06-01 |
Syndromes, disorders and maternal risk factors associated with neural tube defects (IV) |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2008-03-01 |
Syndromes, disorders and maternal risk factors associated with neural tube defects (I) |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2008-03-01 |
Syndromes, disorders and maternal risk factors associated with neural tube defects (II) |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2007-12-01 |
Chromosomal abnormalities associated with neural tube defects (I): full aneuploidy |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2007-12-01 |
Chromosomal abnormalities associated with neural tube defects (II): partial aneuploidy |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2007-12-01 |
Lethal multiple pterygium syndrome associated with omphalocele |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2007-09-01 |
Prenatal diagnosis of arachnoid cysts |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2007-09-01 |
Prenatal diagnosis of iniencephaly |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2007-06-01 |
Prenatal diagnosis of atypical facial clefting should alert amniotic band syndrome and prompt a search for associated amniotic bands and other structural anomalies |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2007-06-01 |
Syndromes and disorders associated with omphalocele (I): Beckwith-Wiedemann syndrome |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2007-06-01 |
Syndromes and disorders associated with omphalocele (II): OEIS complex and pentalogy of Cantrell |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2007-06-01 |
Syndromes and disorders associated with omphalocele (III): single gene disorders, neural tube defects, diaphragmatic defects and others |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2007-06-01 |
Thoraco-omphalopagus conjoined twins associated with omphalocele and an umbilical cord cyst |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2007-03-01 |
Chromosomal abnormalities associated with omphalocele |
Chih-Ping Chen; |
|
[生物醫學研究所] 期刊論文 |
2009-12-01 |
Prenatal diagnosis of monosomy 17p (17p13.3→pter) associated with polyhydramnios, intrauterine growth restriction, ventriculomegaly and Miller-Dieker lissencephaly syndrome in a fetus |
Chin-Yi Lin; Chih-Ping Chen; Chiung-Ling Liau; Pen-Hua Su; Teng-Fu Tsao; Tung-Yao Chang; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-03-01 |
Placenta percreta presenting as a pinhole uterine rupture and acute abdomen |
Fang-Yu Hung; Pu-Tsui Wang; Shun-Long Weng; Chih-Ping Chen |
|
[生物醫學研究所] 期刊論文 |
2008-06-01 |
Omental trophoblastic implant with hemoperitoneum as a sequela of suction dilatation and curettage |
Hong-Ming Wu; Chih-Ping Chen; Kuo-Ming Chang; Shing-Jyh Chang |
|
[生物醫學研究所] 期刊論文 |
2010-12-01 |
Polysomnographic characteristics in patients with mucopolysaccharidoses |
Hsiang-Yu Lin; Ming-Ren Chen; Ching-Chi Lin; Chih-Ping Chen; Dar-Shong Lin; Chih-Kuang Chuang; Dau-Ming Niu; Jui-Hung Chang; Hung-Chang Lee; Shuan-Pei Lin |
|
[生物醫學研究所] 期刊論文 |
2010-06-01 |
Epicatechin gallate decreases the viability and subsequent embryonic development of mouse blastocysts |
Hsiao-Chen Tu; Chih-Ping Chen; Wen-Hsiung Chan |
|
[生物醫學研究所] 期刊論文 |
2007-09-01 |
Typical body wall defect associated with craniofacial anomalies and amniotic bands diagnosed in early pregnancy |
Hsiao-En Cindy Chen; Chih-Ping Chen; Chin-Yuan Hsu; Wayseen Wang |
|
[生物醫學研究所] 期刊論文 |
2010-07-01 |
Single-nucleotide polymorphisms in chromosome 3p14.1-3p14.2 are associated with susceptibility of type 2 diabetes with cataract |
Hui-Ju Lin; Yu-Chuen Huang; Jane-Ming Lin; Jer-Yuarn Wu; Liuh-An Chen; Chao-Jen Lin; Yung-Ping Tsui; Chih-Ping Chen; Fuu-Jen Tsai |
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[生物醫學研究所] 期刊論文 |
2008-09-01 |
Ectopic pregnancy with oral contraceptive use |
Hung-Hung Lin; Ming-Chao Huang; Chen-Ju Lin; Chih-Ping Chen. |
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[生物醫學研究所] 期刊論文 |
2009-06-01 |
Association of interleukin-10 A-592C polymorphism in Taiwanese children with Kawasaki disease. |
Kai-Chung Hsueh; Ying-Ju Lin; Jeng-Sheng Chang; Lei Wan; Yu-Hsin Tsai; Chang-Hai Tsai; Chih-Ping Chen; Fuu-Jen Tsai |
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[生物醫學研究所] 期刊論文 |
2008-03-01 |
Association of vascular endothelial growth factor C-634 G polymorphism in Taiwanese children with Kawasaki disease |
Kai-Chung Hsueh; Ying-Ju Lin; Jeng-Sheng Chang; Lei Wan; Yuhsin Tsai; Chang-Hai Tsai; Chih-Ping Chen; Fuu-Jen Tsai |
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[生物醫學研究所] 期刊論文 |
2008-06-01 |
Hematocolpometra associated with an imperforate hymen and acute urinary retention mimicking a pelvic mass |
Kuang-Pin Hsu; Chih-Ping Chen; Shu-Chin Chien; Chin-Yuan Hsu |
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[生物醫學研究所] 期刊論文 |
2007-12-01 |
Growth hormone (GH) receptor C.1319 G>T polymorphism, but not exon 3 retention or deletion is associated with better first-year growth response to GH therapy in patients with GH deficiency |
Lei Wan; Wei-Cheng Chen; Yuhsin Tsai; Yu-Tsun Kao; Yao-Yuan Hsieh; Cheng-Chun Lee; Chang-Hai Tsai; Chih-Ping Chen; Fuu-Jen Tsai |
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[生物醫學研究所] 期刊論文 |
2007-05-01 |
Proinflammatory macrophage migratory inhibition factor and interleukin-6 are concentrated in pleural effusion of human fetuses with prenatal chylothorax |
Ming Chen; Chang-Yao Hsieh; Jin-Chung Shih; Chia-Hung Chou; Gwo-Chin Ma; Tze-Ho Chen; Tsung-Hsien Lee; Horng-Der Tsai; Alan D. Cameron; Chih-Ping Chen |
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[生物醫學研究所] 期刊論文 |
2009-07-01 |
A case of restrictive dermopathy with complete chorioamniotic membrane separation caused by a novel homozygous nonsense mutation in the ZMPSTE24 gene |
Ming Chen; Hsiang-Hsu Kuo; Yi-Chen Huang; Yu-Yuan Ke; Shun-Ping Chang; Chih-Ping Chen; Dong-Jay Lee; Meng-Luen Lee; Mei-Hui Lee; Tze-Ho Chen; Chia-Hsiang Chen; Hui-Mei Lin; Chin-San Liu; Gwo-Chin Ma |
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[生物醫學研究所] 期刊論文 |
2008-06-01 |
Huge pelvic mass, cutaneous and vaginal fistulas, and bilateral hydronephrosis: a rare presentation of actinomycosis with a good response to conservative treatment and with long-term sequelae of renal atrophy and hydronephrosis |
Pu-Tsui Wang; Shey-Chiang Su; Fang-Yu Hung; Shun-Long Weng; Chih-Ping Chen |
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[生物醫學研究所] 期刊論文 |
2011-09-01 |
Spatiotemporal expression of SERPINE2 in the human placenta and its role in extravillous trophoblast migration and invasion |
Schu-Rern Chern; Sheng-Hsiang Li,; Chien-Ling Chiu; Hsiao-Ho Chang; Chih-Ping Chen; Edmund I Tsuen Chen |
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[生物醫學研究所] 期刊論文 |
2008-02-01 |
Gene dosage change of TPTE and BAGE2 and breakpoint analysis in Robertsonian Down syndrome |
Sheng-Wen Shaw; Chih-Ping Chen; Po-Jen Cheng; Tzu-Hao Wang; Jia-Woei Hou; Cheng-Tao Lin; Shuenn-Dhy Chang; Hsiao-Lin Hwa; Ju-Li Lin; An-Shine Chao; Yung-Kuei Soong; Fon-Jou Hsieh |
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[生物醫學研究所] 期刊論文 |
2008-06-01 |
First- and second-trimester Down syndrome screening: current strategies and clinical guidelines |
Sheng-Wen Shaw; Jenn-Jeih Hsu; Chien-Nan Lee; Ching-Hua Hsiao; Chih-Ping Chen; T'sang-T'ang Hsieh; Po-Jen Cheng |
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[生物醫學研究所] 期刊論文 |
2008-09-01 |
Rapid prenatal diagnosis of spinal muscular atrophy by denaturing high-performance liquid chromatography system |
Sheng-Wen Shaw; Po-Jen Cheng; Shuenn-Dhy Chang; Yu-Ting Lin; Chia-Cheng Hung; Chih-Ping Chen; Yi-Ning Su |
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[生物醫學研究所] 期刊論文 |
2010-03-01 |
Second-trimester maternal serum quadruple test for Down syndrome screening: a Taiwanese population-based study |
Sheng-Wen Steven Shaw; Shin-Yu Lin; Chia-Hui Lin; Yi-Ning Su; Po-Jen Cheng; Chien-Nan Lee; Chih-Ping Chen |
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[生物醫學研究所] 期刊論文 |
2010-12-01 |
Stroke during pregnancy and puerperium: clinical perspectives |
Shih-Jung Cheng; Pei-Hao Chen; Lu-An Chen; Chih-Ping Chen |
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[生物醫學研究所] 期刊論文 |
2009-09-01 |
Prenatal diagnosis of mos45,X/46,X,+mar in a fetus with normal male external genitalia and a literature review |
Shu-Chin Chien; Chih-Ping Chen; Chyi-Chyang Lin; Li-Chia Huang; Cheng-Tiao Hsieh; Fuu-Jen Tsai |
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[生物醫學研究所] 期刊論文 |
2008-06-01 |
Spontaneous rupture of omental teratoma mimicking a ruptured ovarian teratoma |
Shwu-Shiuang Chen; Chih-Ping Chen; Shu-Chin Chien; Chin-Yuan Hsu |
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[生物醫學研究所] 期刊論文 |
2009-12-01 |
Tension-free vaginal tape-obturator procedure for treatment of severe urodynamic stress incontinence: Subjective and objective outcomes during 2 years of follow-up |
Tsung-Hsien Su; Wen-Chu Huang; Mei-Yu Lee; Tzu-Yin Lin; Hui-Chin Chang; Chih-Ping Chen |
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[生物醫學研究所] 期刊論文 |
2010-12-01 |
Alzheimer's Disease: Aging, Insomnia and Epigenetics |
Tzong-Yuan Wu; Chih-Ping Chen; Tzyy-Rong Jinn |
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[生物醫學研究所] 期刊論文 |
2009-09-01 |
Dual action of memantine in Alzheimer disease: a hypothesis |
Tzong-Yuan Wu; Chih-Ping Chen |
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[生物醫學研究所] 期刊論文 |
2007-07-01 |
Rapid prenatal diagnosis of Duchenne muscular dystrophy with gene duplications by ion-pair reversed-phase high-performance liquid chromatography coupled with competitive multiplex polymerase chain reaction strategy |
Wan-Yi Huang; Chia-Cheng Hung; Chien-Nan Lee; Yi-Ning Su; Chih-Ping Chen |
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[生物醫學研究所] 期刊論文 |
2007-09-01 |
Human gene mutations. Gene symbol: EXT2. Disease: exostoses (multiple) 2 |
Wei-De Lin; Chang-Hai Tsai; Chih-Ping Chen; Fuu-Jen Tsai |
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[生物醫學研究所] 期刊論文 |
2008-10-01 |
Human gene mutations. Gene symbol: LMX1B. Disease: Nail-patella syndrome |
Wei-De Lin; Chih-Ping Chen,; D-Y Wang; Fuu-Jen Tsai. |
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[生物醫學研究所] 期刊論文 |
2007-09-01 |
Human gene mutations. Gene symbol: EXT1. Disease: exostoses (multiple) 1 |
Wei-De Lin; Shuan-Pei Lin; Chih-Ping Chen; Fuu-Jen Tsai |
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[生物醫學研究所] 期刊論文 |
2008-08-01 |
Genetic analysis of mucopolysaccharidosis type VI in Taiwanese patients |
Wei-De Lin; Shuan-Pei Lin; Chung-Hsing Wang; Wuh-Liang Hwu; Chih-Kuang Chuang; Shio-Jean Lin; Yushin Tsai; Chih-Ping Chen; Fuu-Jen Tsai. |
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[生物醫學研究所] 期刊論文 |
2011-04-01 |
RUNX2 mutations in Taiwanese patients with cleidocranial dysplasia |
Wei-De Lin; Shuan-Pei Lin,; Chung-Hsing Wang; Yushin Tsai; Chih-Ping Chen; Fuu-Jen Tsai |
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[生物醫學研究所] 期刊論文 |
2007-09-01 |
Human gene mutations. Gene symbol: GLA. Disease: Fabry disease |
Wei-De Lin; Wuh-Liang Hwu; Su-Chiang Liu; Chih-Ping Chen; Fuu-Jen Tsai |
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[醫學系] 期刊論文 |
2006-01-01 |
CXCR4 expression is associated with pelvic lymph node metastasis in cervical adenocarcinoma. |
Yang Y.C.; Lee Z.Y; Wu C.C; Chen T.C; Chang C.L.; Chen C.P. |
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[生物醫學研究所] 期刊論文 |
2009-03-01 |
The p21 codon 31*C- and DRD2 codon 313*T-related genotypes/alleles, but not XRCC1 codon 399, hOGG1 codon 326, and DRD1-48 polymorphisms, are correlated with the presence of leiomyoma |
Yao-Yuan Hsieh; Chi-Chen Chang; Da-Tian Bau; Fuu-Jen Tsai; Chang-Hai Tsai; Chih-Ping Chen |
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[生物醫學研究所] 期刊論文 |
2008-09-01 |
Effect of exercise training on calpain systems in lean and obese Zucker rats |
Yao-Yuan Hsieh; Chi-Chen Chang; Kung-Hao Hsu; Fuu-Jen Tsai; Chih-Ping Chen; Horng-Der Tsai |
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[生物醫學研究所] 期刊論文 |
2008-05-01 |
XRCC4 codon 247*A and XRCC4 promoter -1394*T related genotypes but not XRCC4 intron 3 gene polymorphism are associated with higher susceptibility for endometriosis |
Yao-Yuan Hsieh; Da-Tian Bau; Chi-Chen Chang; Chang-Hai Tsai; Chih-Ping Chen; Fuu-Jen Tsai |
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[生物醫學研究所] 期刊論文 |
2011-12-01 |
Prenatal diagnosis of a de novo interstitial deletion of chromosome 20q12 in a fetus with complex congenital heart defects, corpus callosum agenesis and intrauterine growth restriction |
Yi-Hui Lin; Chih-Ping Chen; Tze-Chien Chen; Chun-Sen Hsu; Szu-Yuan Chou; Shu-Chin Chien |
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[生物醫學研究所] 期刊論文 |
2008-02-01 |
A/C polymorphism in the interleukin-18 coding region among Taiwanese systemic lupus erythematosus patients |
Ying-Ju Lin; Lei Wan; Jim Jinn-Chyuan Sheu; Chung-Ming Huang; Cheng-Wen Lin; Yu-Ching Lan; Chih-Ho Lai; Chien-Hui Hung; Yuhsin Tsai,; Chang-Hai Tsai; T-H Lin; Chih-Ping Chen; Fuu-Jen Tsai |
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[生物醫學研究所] 期刊論文 |
2010-07-01 |
Single nucleotide polymorphism rs2229634 in the ITPR3 gene is associated with the risk of developing coronary artery aneurysm in children with Kawasaki disease |
Yu-Chuen Huang; Y-J Lin; J-S Chang; S-Y Chen; Lei Wan; Jim Jinn-Chyuan Sheu; Chih-Ho Lai; Wei-Yong Lin; Hsing-Ping Liu; Chih-Ping Chen; Fuu-Jen Tsai |
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[生物醫學研究所] 期刊論文 |
2009-06-01 |
Genome-wide detection of uniparental disomy in a fetus with intrauterine growth restriction using genotyping microarrays |
Yung-Kuei Soong; Tzu-Hao Wang; Yun-Shien Lee; Chih-Ping Chen; Chia-Lin Chang; Szu-Ying Ho; An-Shine Chao; Po-Jen Cheng; Shuenn-Dyh Chang. |
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[生物醫學研究所] 期刊論文 |
2010-06-01 |
Fetal cystic lung lesions: Evaluation with magnetic resonance imaging |
Yu-Peng Liu; Chih-Ping Chen; Shin-Lin Shih; Yi-Fang Chen; Fei-Shih Yang; Su-Chiu Chen |
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[生物醫學研究所] 期刊論文 |
2009-08-01 |
Fetal MRI of hydrometrocolpos with septate vagina and uterus didelphys as well as massive urinary ascites due to cloacal malformation |
Yu-Peng Liu; Chih-Ping Chen |
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[生物醫學研究所] 期刊論文 |
2008-01-01 |
Torsion of a huge ovarian cyst in a 90-year-old woman |
Yu-Yueh Peng; Chih-Ping Chen; Shu-Chin Chien; Jen-Ruei Chen |
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