| [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 |
2012-12-01 |
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 |
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 |
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 |
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 |
2012-12-01 |
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 |
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 |
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 |
2012-11-01 |
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 |
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 |
2012-09-01 |
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 |
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 |
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 |
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 |
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 |
|
| [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 |
2012-09-01 |
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 |
2012-09-01 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
|
| [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 |
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 |
2012-06-01 |
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 |
2012-06-01 |
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 |
2012-06-01 |
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 |
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 |
2012-03-01 |
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 |
2012-03-01 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
2011-12-01 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
|
| [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 |
2011-06-01 |
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 |
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 |
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 |
2011-06-01 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
|
| [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 |
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 |
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 |
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 |
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 |
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 |
2010-09-01 |
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 |
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 |
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 |
2010-09-01 |
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 |
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 |
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 |
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 |
2010-06-01 |
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 |
2010-06-01 |
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 |
|
| [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 |
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 |
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 |
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 |
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 |
2010-03-01 |
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 |
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 |
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 |
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 |
2009-12-01 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
2009-03-01 |
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 |
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 |
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 |
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 |
2008-07-01 |
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 |
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 |
2008-06-01 |
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 |
2008-05-01 |
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 |
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 |
2008-03-01 |
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 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 |
2008-03-01 |
Triploidy and fetal holoprosencephaly |
Chih-Ping Chen; Edison Shieh; Schu-Rern Chern; 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 |
|
| [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 |
|
| [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 |
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 |
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 |
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 |
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 |
2007-03-01 |
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 |
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 |
|
| [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 |
|
| [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 |
|
| [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 |
|
| [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 |
|
| [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 |
|
| [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 |
|
| [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 |
|
| [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 |
|
