| [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 |
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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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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 |
2010-03-01 |
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 |
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| [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 |
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| [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 |
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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 |
2008-01-01 |
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 |
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 |
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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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 |
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| [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 |
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| [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 |
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| [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 |
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 |
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| [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. |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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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 |
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 |
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| [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 |
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| [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 |
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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 |
2007-09-01 |
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 |
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 |
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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| [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 |
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| [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 |
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| [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 |
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| [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 |
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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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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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 |
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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
2008-06-01 |
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. |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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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 |
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| [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 |
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| [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 |
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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 |
2008-09-01 |
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 |
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| [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 |
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| [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. |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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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 |
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 |
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| [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 |
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| [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 |
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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 |
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 |
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 |
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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 |
2008-06-01 |
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 |
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| [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 |
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| [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 |
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| [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 |
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| [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 |
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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 |
2006-08-01 |
Diversity of the CYP21A2 gene: A 6.2-kb TaqI fragment and a 3.2-kb TaqI fragment mistaken as CYP21A1P |
Hsien-Hsiung Lee; Fuu-Jen Tsai; Yann-Jinn Lee; Yuh-Cheng Yang |
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