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Wayseen Wang

Research Profile

Physiology

Procedures

Disorders

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Living Beings

Newborn Infant

Anatomy

Chromosomes, Human, Pair 18

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Publications

TOP 3
Chih-Ping Chen; Li-Feng Chen; Yu-Ting Chen; Schu-Rern Chern; Chen-Chi Lee; Chen-Ju Lin; Jun-Wei Su; Tung-Yao Chang; Peih-Shan Wu; Wayseen Wang
Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization.
Chih-Ping Chen; Schu-Rern Chern; Chin-Yuan Hsu; Jun-Wei Su; Yi-Ning Su; Tao-Yeuan Wang; Wayseen Wang
Placental mesenchymal dysplasia associated with antepartum hemorrhage, subchorionic hematoma, and intrauterine growth restriction.
Chih-Ping Chen; Schu-Rern Chern; Shuan-Pei Lin; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome.

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2013: Chih-Ping Chen; Li-Feng Chen; Yu-Ting Chen; Schu-Rern Chern; Chen-Chi Lee; Chen-Ju Lin; Jun-Wei Su; Tung-Yao Chang; Peih-Shan Wu; Wayseen Wang
Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization.
Gene 2013;519(1):164-8.
2013: Chih-Ping Chen; Schu-Rern Chern; Chin-Yuan Hsu; Jun-Wei Su; Yi-Ning Su; Tao-Yeuan Wang; Wayseen Wang
Placental mesenchymal dysplasia associated with antepartum hemorrhage, subchorionic hematoma, and intrauterine growth restriction.
Taiwanese journal of obstetrics & gynecology 2013;52(1):154-6.
2013: Chih-Ping Chen; Schu-Rern Chern; Shuan-Pei Lin; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome.
Taiwanese journal of obstetrics & gynecology 2013;52(1):152-3.
2013: Chih-Ping Chen; Li-Feng Chen; Yu-Ting Chen; Tsang-Ming Ko; Chen-Chi Lee; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2→q11.21).
Taiwanese journal of obstetrics & gynecology 2013;52(1):147-51.
2013: Chih-Ping Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Ho-Yen Chueh; Meng-Shan Lee; Jun-Wei Su; Yi-Ning Su; Shuenn-Dyh Chang; Wayseen Wang
Discrepancy in the trisomy mosaicism level between cultured amniocytes and uncultured amniocytes in prenatally detected mosaic trisomy 20.
Taiwanese journal of obstetrics & gynecology 2013;52(1):145-6.
2013: Chih-Ping Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Kwui-Shuai Hwang; Shuan-Pei Lin; Her-Young Su; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3→q32.12) associated with abnormal maternal serum biochemistry.
Taiwanese journal of obstetrics & gynecology 2013;52(1):125-8.
2013: Chih-Ping Chen; Yu-Ting Chen; Schu-Rern Chern; Meng-Shan Lee; Shuan-Pei Lin; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistry.
Taiwanese journal of obstetrics & gynecology 2013;52(1):120-4.
2013: Chih-Ping Chen; Schu-Rern Chern; Shuan-Pei Lin; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism.
Taiwanese journal of obstetrics & gynecology 2013;52(1):106-9.
2013: Chih-Ping Chen; Li-Feng Chen; Yu-Ting Chen; Schu-Rern Chern; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis.
Taiwanese journal of obstetrics & gynecology 2013;52(1):97-105.
2013: Chih-Ping Chen; Li-Feng Chen; Yu-Ting Chen; Yi-Yung Chen; Schu-Rern Chern; Jun-Wei Su; Peih-Shan Wu; Wayseen Wang
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold.
Gene 2013;516(1):138-42.
2013: Chih-Ping Chen; Li-Feng Chen; Wen-Lin Chen; Schu-Rern Chern; Jun-Wei Su; Yao-Lung Chang; Peih-Shan Wu; Wayseen Wang
Prenatal diagnosis of partial trisomy 3q (3q27.3→qter) and partial monosomy 14q (14q31.3→qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints.
Gene 2013;516(1):132-7.
2013: Chih-Ping Chen; Ming Chen; Tsang-Ming Ko; Yi-Hui Lin; Gwo-Chin Ma; Yi-Ning Su; Wayseen Wang
Array comparative genomic hybridization characterization of prenatally detected de novo apparently balanced reciprocal translocations with or without genomic imbalance in other chromosomes.
Journal of the Chinese Medical Association : JCMA 2013;76(1):53-6.
2012: Chih-Ping Chen; Schu-Rern Chern; Jun-Wei Su; Yi-Ning Su; Dai-Dyi Town; Peih-Shan Wu; Wayseen Wang
Prenatal diagnosis of an interstitial deletion of 10q (10q11.21 → q21.1): array comparative genomic hybridization characterization and literature review.
Taiwanese journal of obstetrics & gynecology 2012;51(4):672-6.
2012: Chih-Ping Chen; Li-Feng Chen; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
Detection of mosaic balanced homologous acrocentric rearrangement rea(21q21q) in a woman with repeated pregnancy losses.
Taiwanese journal of obstetrics & gynecology 2012;51(4):669-71.
2012: Chih-Ping Chen; Yu-Ting Chen; Schu-Rern Chern; Chen-Wen Pan; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis of trisomy 8 mosaicism.
Taiwanese journal of obstetrics & gynecology 2012;51(4):666-8.
2012: Chih-Ping Chen; Yu-Ting Chen; Jun-Wei Su; Dai-Dyi Town; Shuenn-Dyh Chang; Wayseen Wang
Mosaic isochromosome 20q detected at amniocentesis: a likely cell culture artifact.
Taiwanese journal of obstetrics & gynecology 2012;51(4):663-5.
2012: Chih-Ping Chen; Chen-Yu Chen; Schu-Rern Chern; Jun-Wei Su; Wayseen Wang
First-trimester prenatal diagnosis of Ellis-van Creveld syndrome.
Taiwanese journal of obstetrics & gynecology 2012;51(4):643-8.
2012: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Jun-Wei Su; Tsung-Hsien Su; Wayseen Wang
Alobar holoprosencephaly, cebocephaly, and micropenis in a Klinefelter fetus of a diabetic mother.
Taiwanese journal of obstetrics & gynecology 2012;51(4):630-4.
2012: Chih-Ping Chen; Yu-Ting Chen; Schu-Rern Chern; Tsang-Ming Ko; Jun-Wei Su; Yi-Ning Su; Dai-Dyi Town; Wayseen Wang
Prenatal diagnosis of mosaic tetrasomy 18p.
Taiwanese journal of obstetrics & gynecology 2012;51(4):625-9.
2012: Chih-Ping Chen; Yu-Ting Chen; Schu-Rern Chern; Chen-Wen Pan; Jun-Wei Su; Yi-Ning Su; Peih-Shan Wu; Wayseen Wang
Mosaic trisomy 2 at amniocentesis: prenatal diagnosis and molecular genetic analysis.
Taiwanese journal of obstetrics & gynecology 2012;51(4):603-11.
2012: Chih-Ping Chen; Schu-Rern Chern; Shuan-Pei Lin; Yu-Peng Liu; Shu-Hang Ng; Jun-Wei Su; Shuenn-Dyh Chang; Peih-Shan Wu; Wayseen Wang
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.
European journal of medical genetics 2012;55(11):666-9.
2012: Chih-Ping Chen; Yu-Ting Chen; Schu-Rern Chern; Chen-Chi Lee; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo X;Y translocation.
Taiwanese journal of obstetrics & gynecology 2012;51(3):485-8.
2012: Chih-Ping Chen; Chen-Yu Chen; Wen-Lin Chen; Schu-Rern Chern; Yu-Peng Liu; Yi-Ning Su; Fuu-Jen Tsai; Shun-Long Weng; Pei-Chen Wu; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2012;51(3):481-4.
2012: Chih-Ping Chen; Li-Feng Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Ho-Yen Chueh; Chen-Chi Lee; Meng-Shan Lee; Chen-Wen Pan; Jun-Wei Su; Yi-Ning Su; Dai-Dyi Town; Shuenn-Dyh Chang; Wayseen Wang
Rapid positive confirmation of trisomy 21 mosaicism at amniocentesis by interphase FISH, QF-PCR and aCGH on uncultured amniocytes.
Taiwanese journal of obstetrics & gynecology 2012;51(3):475-80.
2012: Chih-Ping Chen; Yu-Ting Chen; Yi-Yung Chen; Schu-Rern Chern; Jun-Wei Su; Yi-Ning Su; Dai-Dyi Town; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2012;51(3):471-4.
2012: Chih-Ping Chen; Chen-Yu Chen; Schu-Rern Chern; Jun-Wei Su; Yi-Ning Su; Dai-Dyi Town; Wayseen Wang
Pure partial monosomy 3p (3p25.3 → pter): prenatal diagnosis and array comparative genomic hybridization characterization.
Taiwanese journal of obstetrics & gynecology 2012;51(3):435-9.
2012: Chih-Ping Chen; Wen-Lin Chen; Yi-Yung Chen; Schu-Rern Chern; Dai-Dyi Town; Pei-Chen Wu; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2012;51(3):430-4.
2012: Chih-Ping Chen; Li-Feng Chen; Ming Chen; Yu-Ting Chen; Schu-Rern Chern; Alex Hwa-Jiun Hsieh; Alan Hwa-Ruey Hsieh; Dong-Jay Lee; Jun-Wei Su; Shun-Ping Chang; Peih-Shan Wu; Wayseen Wang
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
Taiwanese journal of obstetrics & gynecology 2012;51(3):411-7.
2012: Chih-Ping Chen; Ming Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Meng-Shan Lee; Chen-Wen Pan; Jun-Wei Su; Yi-Ning Su; Shuenn-Dyh Chang; Wayseen Wang
Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase fluorescence in situ hybridization, quantitative fluorescent polymerase chain reaction, and array comparative genomic hybridization on uncultured amniocytes in a pregnancy with fetal pyelectasis.
Taiwanese journal of obstetrics & gynecology 2012;51(3):405-10.
2012: Chih-Ping Chen; Schu-Rern Chern; Ming-Chao Huang; Chun-Heng Pan; Jun-Wei Su; Yi-Ning Su; Tung-Yao Chang; Wayseen Wang
Osteogenesis imperfecta type II: prenatal diagnosis and association with increased nuchal translucency and hypoechogenicity of the cranium.
Taiwanese journal of obstetrics & gynecology 2012;51(2):315-8.
2012: Chih-Ping Chen; Schu-Rern Chern; Fang-Yu Hung; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2012;51(2):312-4.
2012: Chih-Ping Chen; Schu-Rern Chern; Jun-Wei Su; Yi-Ning Su; Tung-Yao Chang; Wayseen Wang
Identification of a deletion mutation in the short flanking repeat region of exon 44 of the COL1A1 gene in a fetus with osteogenesis imperfecta type II.
Taiwanese journal of obstetrics & gynecology 2012;51(2):308-11.
2012: Chih-Ping Chen; Schu-Rern Chern; Jian-Pei Huang; Shuan-Pei Lin; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Uncomplicated vaginal delivery in two consecutive pregnancies carried to term in a woman with osteogenesis imperfecta type I and bisphosphonate treatment before conception.
Taiwanese journal of obstetrics & gynecology 2012;51(2):305-7.
2012: Chih-Ping Chen; Chen-Yu Chen; Schu-Rern Chern; Jun-Wei Su; Yi-Ning Su; Tung-Yao Chang; Wayseen Wang
Osteogenesis imperfecta type I: second-trimester diagnosis and incidental identification of a dominant COL1A1 deletion mutation in the paucisymptomatic father.
Taiwanese journal of obstetrics & gynecology 2012;51(2):276-9.
2012: Chih-Ping Chen; Schu-Rern Chern; Ming-Huei Lin; Shuan-Pei Lin; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Osteogenesis imperfecta type IV: prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcome.
Taiwanese journal of obstetrics & gynecology 2012;51(2):271-5.
2012: Chih-Ping Chen; Yi-Yung Chen; Schu-Rern Chern; Jun-Wei Su; Yi-Ning Su; Tung-Yao Chang; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2012;51(2):266-70.
2012: Chih-Ping Chen; Ming Chen; Yu-Ting Chen; Schu-Rern Chern; Jian-Pei Huang; Chen-Chi Lee; Gwo-Chin Ma; Jun-Wei Su; Yi-Ning Su; Dai-Dyi Town; Shun-Ping Chang; Wayseen Wang
Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
Taiwanese journal of obstetrics & gynecology 2012;51(2):245-52.
2012: Chih-Ping Chen; Chin-Yuan Hsu; Yu-Peng Liu; Fuu-Jen Tsai; Tung-Yao Chang; Pei-Chen Wu; Wayseen Wang
Persistent cloaca presenting with a perineal cyst: Prenatal ultrasound and magnetic resonance imaging findings.
Journal of the Chinese Medical Association : JCMA 2012;75(4):190-3.
2012: Chih-Ping Chen; Schu-Rern Chern; Ming-Chao Huang; Yu-Peng Liu; Jin-Chung Shih; Jun-Wei Su; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2012;51(1):139-42.
2012: Chih-Ping Chen; Li-Feng Chen; Ming Chen; Wen-Lin Chen; Yu-Ting Chen; Yi-Yung Chen; Gwo-Chin Ma; Jun-Wei Su; Yi-Ning Su; Fuu-Jen Tsai; Shun-Ping Chang; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2012;51(1):134-8.
2012: Chih-Ping Chen; Wen-Lin Chen; Yi-Yung Chen; Chin-Yuan Hsu; Tsang-Ming Ko; Chen-Wen Pan; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2012;51(1):129-33.
2012: Chih-Ping Chen; Yi-Yung Chen; Schu-Rern Chern; Jun-Wei Su; Yi-Ning Su; Chih-Long Chang; Wayseen Wang
Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification using uncultured amniocytes in pregnancy with major fetal structural abnormalities.
Taiwanese journal of obstetrics & gynecology 2012;51(1):123-8.
2012: Chih-Ping Chen; Chen-Yu Chen; Schu-Rern Chern; Fuu-Jen Tsai; Tao-Yeuan Wang; Tung-Yao Chang; Pei-Chen Wu; Wayseen Wang
Short rib-polydactyly syndrome type II (Majewski): prenatal diagnosis, perinatal imaging findings and molecular analysis of the NEK1 gene.
Taiwanese journal of obstetrics & gynecology 2012;51(1):100-5.
2012: Chih-Ping Chen; Li-Feng Chen; Meng-Shan Lee; Shuan-Pei Lin; Yi-Ning Su; Dai-Dyi Town; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
Rapid aneuploidy diagnosis of partial trisomy 7q (7q34→qter) and partial monosomy 10q (10q26.12→qter) by array comparative genomic hybridization using uncultured amniocytes.
Taiwanese journal of obstetrics & gynecology 2012;51(1):93-9.
2012: Chih-Ping Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Hsu-Kuang Huang; Chen-Chi Lee; Jun-Wei Su; Yi-Ning Su; Dai-Dyi Town; Wayseen Wang
Trisomy 7 mosaicism at amniocentesis: interphase FISH, QF-PCR, and aCGH analyses on uncultured amniocytes for rapid distinguishing of true mosaicism from pseudomosaicism.
Taiwanese journal of obstetrics & gynecology 2012;51(1):77-82.
2012: Chih-Ping Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Szu-Yuan Chou; Yi-Hui Lin; Yi-Ning Su; Dai-Dyi Town; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2012;51(1):71-6.
2012: C-P Chen; W-L Chen; Schu-Rern Chern; Y-L Huang; C-C Lee; Shuan-Pei Lin; J-W Su; Wayseen Wang
De novo satellited 2q associated with corpus callosum dysgenesis, short stature, mental retardation and developmental delay.
Genetic counseling (Geneva, Switzerland) 2012;23(4):497-503.
2012: C-P Chen; Schu-Rern Chern; C-C Lee; Shuan-Pei Lin; J-W Su; Y-N Su; Wayseen Wang
Partial trisomy 1q (1q42.13-->qter) and partial monosomy 6q (6q27-->qter) in a girl with single median maxillary central incisor, corpus callosum dysgenesis and developmental delay.
Genetic counseling (Geneva, Switzerland) 2012;23(4):447-55.
2012: C P Chen; M R Chen; Schu-Rern Chern; Meng-Shan Lee; Shuan-Pei Lin; Y P Liu; J W Su; Y N Su; Wayseen Wang
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.
Genetic counseling (Geneva, Switzerland) 2012;23(3):405-13.
2012: C P Chen; Schu-Rern Chern; Shuan-Pei Lin; J W Su; Y N Suo; Wayseen Wang
Identification of a missense mutation of c.3064G>A, Gly1022Ser in exon 43 of COL1A1 gene in a girl with osteogenesis imperfecta type III.
Genetic counseling (Geneva, Switzerland) 2012;23(3):359-65.
2012: Chih-Ping Chen; Yann-Jang Chen; Schu-Rern Chern; C-H Hsu; Shuan-Pei Lin; Chen-Wen Pan; J-W Su; Wayseen Wang
Pure distal 11q deletion without additional genomic imbalances in a female infant with Jacobsen syndrome and a de novo unbalanced reciprocal translocation.
Genetic counseling (Geneva, Switzerland) 2012;23(2):223-9.
2012: Chih-Ping Chen; Schu-Rern Chern; Shuan-Pei Lin; J-W Su; Y-N Su; Dai-Dyi Town; Wayseen Wang
Pure distal 9p deletion in a female infant with cerebral palsy.
Genetic counseling (Geneva, Switzerland) 2012;23(2):215-21.
2012: Chih-Ping Chen; Y-T Chen; C Leung; H-M Lin; Shuan-Pei Lin; J-W Su; Y-N Su; Wayseen Wang
Partial monosomy 9p (9p22.2-->pter) and partial trisomy 18q (18q21.32-->qter) in a female infant with anorectal malformations.
Genetic counseling (Geneva, Switzerland) 2012;23(2):201-6.
2012: Chih-Ping Chen; M-R Chen; Yann-Jang Chen; Schu-Rern Chern; Meng-Shan Lee; Shuan-Pei Lin; J-W Su; Wayseen Wang
Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactyly.
Genetic counseling (Geneva, Switzerland) 2012;23(2):195-200.
2012: Chih-Ping Chen; L J Hsu; Dar-Shong Lin; Shuan-Pei Lin; Y P Liu; Wayseen Wang
Clinical imaging findings in a girl with Hutchinson-Gilford progeria syndrome.
Genetic counseling (Geneva, Switzerland) 2012;23(1):1-7.
2011: Chih-Ping Chen; Schu-Rern Chern; Chin-Yuan Hsu; Maw-Shuan Lee; Yu-Peng Liu; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2011;50(4):561-3.
2011: Chih-Ping Chen; Yi-Yung Chen; Jun-Wei Su; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2011;50(4):558-60.
2011: Chih-Ping Chen; Li-Feng Chen; Schu-Rern Chern; Chin-Yuan Hsu; Yu-Peng Liu; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis of a de novo 17p13.1 microduplication in a fetus with ventriculomegaly and lissencephaly.
Taiwanese journal of obstetrics & gynecology 2011;50(4):554-7.
2011: Chih-Ping Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Fang-Yu Hung; Chen-Chi Lee; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis of mosaic trisomy 9.
Taiwanese journal of obstetrics & gynecology 2011;50(4):549-53.
2011: Chih-Ping Chen; Li-Feng Chen; Wen-Lin Chen; Yu-Ting Chen; Yi-Yung Chen; Schu-Rern Chern; Jun-Wei Su; Yi-Ning Su; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2011;50(4):506-11.
2011: Chih-Ping Chen; Ming Chen; Yu-Ting Chen; Schu-Rern Chern; Hsu-Kuang Huang; Chen-Chi Lee; Pei-Ying Ling; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
Taiwanese journal of obstetrics & gynecology 2011;50(4):492-8.
2011: Chih-Ping Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Chin-Yuan Hsu; Chen-Chi Lee; Yi-Ning Su; Wayseen Wang
Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy.
Taiwanese journal of obstetrics & gynecology 2011;50(4):485-91.
2011: Chih-Ping Chen; Chen-Yu Chen; Li-Feng Chen; Schu-Rern Chern; Chen-Wen Pan; Pei-Chen Wu; Wayseen Wang
Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of the left wrist and aplasia of the left thumb.
Taiwanese journal of obstetrics & gynecology 2011;50(4):479-84.
2011: Chih-Ping Chen; Hsiao-En Cindy Chen; Chin-Yuan Hsu; Alex Hwa-Jiun Hsieh; Alan Hwa-Ruey Hsieh; Jun-Wei Su; Wayseen Wang
Conjoined twins detected in the first trimester: a review.
Taiwanese journal of obstetrics & gynecology 2011;50(4):424-31.
2011: Chih-Ping Chen; Wen-Lin Chen; Yu-Ting Chen; Lee James Hsu; Yi-Ning Su; Wayseen Wang
Prenatal diagnosis of directly transmitted benign 4q12-q13.1 quadruplication associated with tandem segmental amplifications of the LPHN3 gene.
Taiwanese journal of obstetrics & gynecology 2011;50(3):401-4.
2011: Chih-Ping Chen; Schu-Rern Chern; Yi-Ning Su; Pei-Chen Wu; Wayseen Wang
Prenatal diagnosis of microvillus inclusion disease.
Taiwanese journal of obstetrics & gynecology 2011;50(3):399-400.
2011: Chih-Ping Chen; Ming Chen; Wen-Lin Chen; Jain-Pei Huang; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation.
Taiwanese journal of obstetrics & gynecology 2011;50(3):394-8.
2011: Chih-Ping Chen; Yu-Ting Chen; Schu-Rern Chern; Meng-Shan Lee; Shin-Yu Lin; Yi-Ning Su; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2011;50(3):390-3.
2011: Chih-Ping Chen; Li-Feng Chen; Yu-Ting Chen; Schu-Rern Chern; Adam Hwa-Ming Hsieh; Chin-Yuan Hsu; Yi-Hui Lin; Yu-Peng Liu; Yi-Ning Su; Heng-Kien Au; Pei-Chen Wu; Wayseen Wang
Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3).
Taiwanese journal of obstetrics & gynecology 2011;50(3):359-65.
2011: Chih-Ping Chen; Yu-Ting Chen; Yi-Yung Chen; Schu-Rern Chern; Chen-Chi Lee; Yu-Peng Liu; Yi-Ning Su; Pei-Chen Wu; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2011;50(3):345-52.
2011: Chih-Ping Chen; Yu-Ting Chen; Schu-Rern Chern; Chen-Chi Lee; Hung-Hung Lin; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
De novo duplication of Xq22.1→q24 with a disruption of the NXF gene cluster in a mentally retarded woman with short stature and premature ovarian failure.
Taiwanese journal of obstetrics & gynecology 2011;50(3):339-44.
2011: Chih-Ping Chen; Ming Chen; Yu-Ting Chen; Schu-Rern Chern; Yi-Ju Pan; Yi-Ning Su; Fuu-Jen Tsai; Wayseen Wang
Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review.
Taiwanese journal of obstetrics & gynecology 2011;50(3):331-8.
2011: Chih-Ping Chen; Chin-Yuan Hsu; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
Prenatal ultrasound demonstration of limb-body wall complex with megacystis.
Taiwanese journal of obstetrics & gynecology 2011;50(2):258-60.
2011: Chih-Ping Chen; Li-Feng Chen; Ming Chen; Yi-Yung Chen; Gwo-Chin Ma; Shun-Ping Chang; Pei-Chen Wu; Wayseen Wang
Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome.
Taiwanese journal of obstetrics & gynecology 2011;50(2):253-7.
2011: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo interstitial deletion of chromosome 20p.
Taiwanese journal of obstetrics & gynecology 2011;50(2):249-52.
2011: Chih-Ping Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Chi-Hsin Chiang; Chen-Chi Lee; Jui-Der Liou; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis.
Taiwanese journal of obstetrics & gynecology 2011;50(2):245-8.
2011: Chih-Ping Chen; Chen-Yu Chen; Shuan-Pei Lin; Yu-Peng Liu; Shin-Lin Shih; Fuu-Jen Tsai; Jeng-Daw Tsai; Pei-Chen Wu; Wayseen Wang
Galloway-Mowat syndrome: prenatal ultrasound and perinatal magnetic resonance imaging findings.
Taiwanese journal of obstetrics & gynecology 2011;50(2):212-6.
2011: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Ming-Huei Lin; Chen-Wen Pan; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization.
Taiwanese journal of obstetrics & gynecology 2011;50(2):205-11.
2011: Chih-Ping Chen; Li-Feng Chen; Ming Chen; Wen-Lin Chen; Schu-Rern Chern; Chen-Wen Pan; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.
Taiwanese journal of obstetrics & gynecology 2011;50(2):188-95.
2011: Chih-Ping Chen; Yu-Ting Chen; Schu-Rern Chern; Yau-Kun Kuo; Yi-Ning Su; Dai-Dyi Town; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2011;50(2):182-7.
2011: Chih-Ping Chen; Tao-Yeuan Wang; Pei-Chen Wu; Fuu-Jen Tsai; Wayseen Wang
Pathological characterization of a malformed umbilical cord associated with body stalk anomaly.
Taiwanese journal of obstetrics & gynecology 2011;50(1):126-8.
2011: 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
Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations.
Taiwanese journal of obstetrics & gynecology 2011;50(1):85-94.
2011: 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
Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
Taiwanese journal of obstetrics & gynecology 2011;50(1):67-73.
2011: 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
Unbalanced reciprocal translocations at amniocentesis.
Taiwanese journal of obstetrics & gynecology 2011;50(1):48-57.
2011: Chih-Ping Chen; Yann-Jang Chen; Schu-Rern Chern; Meng-Shan Lee; Shuan-Pei Lin; Fuu-Jen Tsai; Wayseen Wang
Pure interstitial duplication of chromosome 7q (7q31.2-->q33) in a 4-year-old girl with growth restriction, short stature, speech delay and intellectual disability.
Genetic counseling (Geneva, Switzerland) 2011;22(4):425-30.
2011: Chih-Ping Chen; M Chen; Yann-Jang Chen; Schu-Rern Chern; Chen-Chi Lee; Shuan-Pei Lin; Y P Liu; Y N Su; Fuu-Jen Tsai; T Y Wang; Wayseen Wang
Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy facial asymmetry psychomotor retardation kyphoscoliosis dermatofibrosarcoma and multiple exostoses.
Genetic counseling (Geneva, Switzerland) 2011;22(3):273-80.
2011: Chih-Ping Chen; L F Chen; Schu-Rern Chern; Shuan-Pei Lin; Y N Su; Fuu-Jen Tsai; P C Wu; Wayseen Wang
A 24.2-Mb deletion of 4q12 --> q21.21 characterized by array CGH in a 131/2-year-old girl with short stature, mental retardation, developmental delay, hyperopia, exotropia, enamel defects, delayed tooth eruption and delayed puberty.
Genetic counseling (Geneva, Switzerland) 2011;22(3):255-61.
2010: 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
Recurrent distal 16q duplication and terminal 22q deletion: prenatal diagnosis and genetic counseling.
Taiwanese journal of obstetrics & gynecology 2010;49(4):544-7.
2010: 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
Partial trisomy 10q (10q25.1 →qter) and partial monosomy 13q (13q34→qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization.
Taiwanese journal of obstetrics & gynecology 2010;49(4):539-43.
2010: 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
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.
Taiwanese journal of obstetrics & gynecology 2010;49(4):506-12.
2010: 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
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8.
Taiwanese journal of obstetrics & gynecology 2010;49(4):500-5.
2010: 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
Microvillus inclusion disease: prenatal ultrasound findings, molecular diagnosis and genetic counseling of congenital diarrhea.
Taiwanese journal of obstetrics & gynecology 2010;49(4):487-94.
2010: Chih-Ping Chen; Yi-Ning Su; Chin-Yuan Hsu; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Po-Tsang Chen; Wayseen Wang
Ellis-van Creveld syndrome: prenatal diagnosis, molecular analysis and genetic counseling.
Taiwanese journal of obstetrics & gynecology 2010;49(4):481-6.
2010: 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
Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
Taiwanese journal of obstetrics & gynecology 2010;49(4):473-80.
2010: 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
Balanced reciprocal translocations detected at amniocentesis.
Taiwanese journal of obstetrics & gynecology 2010;49(4):455-67.
2010: 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
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.
Taiwanese journal of obstetrics & gynecology 2010;49(3):387-9.
2010: Chih-Ping Chen; Yu-Peng Liu; Tung-Yao Chang; Fuu-Jen Tsai; Chen-Yu Chen; Pei-Chen Wu; Teresa Hsiao-Tien Chen; Wayseen Wang
Prenatal diagnosis of persistent cloaca with hydrometrocolpos and ascites by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy.
Taiwanese journal of obstetrics & gynecology 2010;49(3):385-6.
2010: 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
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22.
Taiwanese journal of obstetrics & gynecology 2010;49(3):381-4.
2010: 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
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21.
Taiwanese journal of obstetrics & gynecology 2010;49(3):377-80.
2010: 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
Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses.
Taiwanese journal of obstetrics & gynecology 2010;49(3):341-50.
2010: Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Yuh-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
Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses.
Taiwanese journal of obstetrics & gynecology 2010;49(3):333-40.
2010: Chih-Ping Chen; Yung-Ting Kuo; Shuan-Pei Lin; Yi-Ning Su; Yann-Jang Chen; Rui-Yuan Hsueh; Yi-Hui Lin; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Wayseen Wang
Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
Taiwanese journal of obstetrics & gynecology 2010;49(3):327-32.
2010: 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
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.
Taiwanese journal of obstetrics & gynecology 2010;49(3):320-6.
2010: Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Wen-Ling Chen; Wayseen Wang
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.
European journal of medical genetics 2010;53(5):329-32.
2010: Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Yann-Jang Chen; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
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.
European journal of medical genetics 2010;53(4):217-20.
2010: 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
Fetal magnetic resonance imaging demonstration of central nervous system abnormalities and polydactyly associated with Joubert syndrome.
Taiwanese journal of obstetrics & gynecology 2010;49(2):243-6.
2010: Chih-Ping Chen; Schu-Rern Chern; Chia-Hsun Wu; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
Detection of balanced homologous acrocentric rearrangement rea(14q14q) and low-grade X-chromosome mosaicism in a couple with repeated pregnancy losses.
Taiwanese journal of obstetrics & gynecology 2010;49(2):239-42.
2010: Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Hsiao-En Cindy Chen; Shu-Shien Chiang; Wayseen Wang
Mosaic tetrasomy 12p with discrepancy between fetal tissues and extraembryonic tissues: molecular analysis and possible mechanism of formation.
Taiwanese journal of obstetrics & gynecology 2010;49(2):235-8.
2010: Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Chen-Yu Chen; Fuu-Jen Tsai; Yu-Peng Liu; Schu-Rern Chern; Pei-Chen Wu; Hsiao-En Cindy Chen; Wayseen Wang
Apert syndrome associated with upper airway obstruction and gastroesophageal reflux inducing polyhydramnios in the third trimester.
Taiwanese journal of obstetrics & gynecology 2010;49(2):231-4.
2010: Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Tao-Yeuan Wang; Fuu-Jen Tsai; Hung-Hung Lin; Pei-Chen Wu; Wayseen Wang
Detection and comparison of cytomegalovirus DNA levels in amniotic fluid and fetal ascites in a second-trimester fetus with massive ascites, hyperechogenic bowel, ventriculomegaly and intrauterine growth restriction.
Taiwanese journal of obstetrics & gynecology 2010;49(2):206-10.
2010: Chih-Ping Chen; Chyi-Chyang Lin; Yi-Ning Su; Fuu-Jen Tsai; Ju-Ting Chen; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town; Li-Feng Chen; Pei-Chen Wu; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2010;49(2):188-91.
2010: Chih-Ping Chen; Yi-Ning Su; Chin-Yuan Hsu; Pei-Ying Ling; Fuu-Jen Tsai; Schu-Rern Chern; Pei-Chen Wu; Hsiao-En Cindy Chen; Wayseen Wang
Second-trimester molecular prenatal diagnosis of sporadic Apert syndrome following sonographic findings of mild ventriculomegaly and clenched hands mimicking trisomy 18.
Taiwanese journal of obstetrics & gynecology 2010;49(1):129-32.
2010: 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
Abnormally flat facial profile on two- and three-dimensional ultrasound and array comparative genomic hybridization for the diagnosis of Pallister-Killian syndrome.
Taiwanese journal of obstetrics & gynecology 2010;49(1):124-8.
2010: Chih-Ping Chen; Yi-Ning Su; Fuu-Jen Tsai; Schu-Rern Chern; Chin-Yuan Hsu; Ming-Chao Huang; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2010;49(1):120-3.
2010: Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Chin-Yuan Hsu; Chen-Chi Lee; Wayseen Wang
Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21 --> q11.23 by array comparative genomic hybridization.
Taiwanese journal of obstetrics & gynecology 2010;49(1):117-9.
2010: Chih-Ping Chen; Yu-Peng Liu; Shaun-Pei Lin; Ming Chen; Fuu-Jen Tsai; Yu-Ting Chen; Li-Feng Chen; Jonathan Kwei Hwang; Wayseen Wang
Ventriculomegaly, intrauterine growth restriction, and congenital heart defects as salient prenatal sonographic findings of Miller-Dieker lissencephaly syndrome associated with monosomy 17p (17p13.2 --> pter) in a fetus.
Taiwanese journal of obstetrics & gynecology 2010;49(1):81-6.
2010: 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
Unbalanced and balanced heterologous acrocentric rearrangements involving chromosome 21 at amniocentesis.
Taiwanese journal of obstetrics & gynecology 2010;49(1):62-8.
2010: Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Fuu-Jen Tsai; Tao-Yeuan Wang; Hung-Hung Lin; Wayseen Wang
Prenatal diagnosis of X-linked myotubular myopathy.
Prenatal diagnosis 2010;30(2):177-9.
2009: Chih-Ping Chen; Maw-Shuan Lee; Fuu-Jen Tsai; Ming-Chao Huang; Schu-Rern Chern; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2009;48(4):446-50.
2009: 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
Terminal 2q deletion and distal 15q duplication: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes.
Taiwanese journal of obstetrics & gynecology 2009;48(4):441-5.
2009: Chih-Ping Chen; Yi-Ning Su; Tung-Yao Chang; Schu-Rern Chern; Fuu-Jen Tsai; Jonathan Kwei Hwang; Wayseen Wang
22q11.2 microdeletion in a fetus with double-outlet right ventricle, pulmonary stenosis and a ventricular septal defect: prenatal diagnosis by array comparative genomic hybridization.
Taiwanese journal of obstetrics & gynecology 2009;48(4):437-40.
2009: Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Wayseen Wang
Trisomy 13 mosaicism associated with cyclopia and cystic hygroma.
Taiwanese journal of obstetrics & gynecology 2009;48(4):434-6.
2009: Chin-Yi Lin; Chih-Ping Chen; Chiung-Ling Liau; Pen-Hua Su; Teng-Fu Tsao; Tung-Yao Chang; Wayseen Wang
Prenatal diagnosis of monosomy 17p (17p13.3-->pter) associated with polyhydramnios, intrauterine growth restriction, ventriculomegaly, and Miller-Dieker lissencephaly syndrome in a fetus.
Taiwanese journal of obstetrics & gynecology 2009;48(4):408-11.
2009: Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Shu-Shien Chiang; Chen-Chi Lee; Wayseen Wang
Down syndrome due to unbalanced homologous acrocentric rearrangements and its recurrence in subsequent pregnancies: prenatal diagnosis by amniocentesis.
Taiwanese journal of obstetrics & gynecology 2009;48(4):403-7.
2009: 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
Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis.
Taiwanese journal of obstetrics & gynecology 2009;48(4):389-99.
2009: Chih-Ping Chen; Yi-Ning Su; Tung-Yao Chang; Yu-Peng Liu; Fuu-Jen Tsai; Jonathan Kwei Hwang; Wayseen Wang
Prenatal magnetic resonance imaging, ultrasound imaging findings and genetic analysis of concomitant rhabdomyomas and cerebral tuberous sclerosis.
Taiwanese journal of obstetrics & gynecology 2009;48(3):327-31.
2009: Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Chin-Yuan Hsu; Kevin Ko; Wayseen Wang
Prenatal diagnosis and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly.
Taiwanese journal of obstetrics & gynecology 2009;48(3):323-6.
2009: Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Hung-Hung Lin; Chen-Wen Pan; Wayseen Wang
Prenatal diagnosis and molecular analysis of trisomy 13 mosaicism.
Taiwanese journal of obstetrics & gynecology 2009;48(3):321-2.
2009: Chih-Ping Chen; Yu-Peng Liu; Fuu-Jen Tsai; Chen-Yu Chen; Hung-Hung Lin; Pei-Chen Wu; Wayseen Wang
Concomitant craniorachischisis and omphalocele in a male fetus: prenatal magnetic resonance imaging findings and literature review.
Taiwanese journal of obstetrics & gynecology 2009;48(3):286-91.
2009: Chih-Ping Chen; Fuu-Jen Tsai; Schu-Rern Chern; Tung-Yao Chang; Chin-Yuan Hsu; Hung-Hung Lin; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2009;48(1):84-7.
2009: 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
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.
European journal of medical genetics 2009;52(1):59-61.
2008: Chih-Ping Chen; Chin-Yuan Tzen; Chen-Yu Chen; Fuu-Jen Tsai; Wayseen Wang
Concomitant exencephaly and limb defects associated with pentalogy of Cantrell.
Taiwanese journal of obstetrics & gynecology 2008;47(4):476-7.
2008: Chih-Ping Chen; Fuu-Jen Tsai; Chen-Yu Chen; Hung-Hung Lin; Wayseen Wang
Limb-body wall complex with craniofacial defects after ovarian stimulation.
Taiwanese journal of obstetrics & gynecology 2008;47(4):474-5.
2008: Chih-Ping Chen; Tzu-Hao Wang; Chyi-Chyang Lin; Fuu-Jen Tsai; Lie-Jiau Hsieh; Wayseen Wang
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.
Journal of the Formosan Medical Association = Taiwan yi zhi 2008;107(10):822-6.
2008: Chih-Ping Chen; Shuan-Pei Lin; Fuu-Jen Tsai; Tzu-Hao Wang; Schu-Rern Chern; Wayseen Wang
Characterization of a de novo unbalanced Y;autosome translocation in a 45,X mentally retarded male and literature review.
Fertility and sterility 2008;90(4):1198.e11-8.
2008: Chih-Ping Chen; Yann-Jang Chen; Schu-Rern Chern; Fuu-Jen Tsai; Hung-Hung Lin; Chen-Chi Lee; Wayseen Wang
Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele.
Prenatal diagnosis 2008;28(9):865-7.
2008: Chih-Ping Chen; Shuan-Pei Lin; Fuu-Jen Tsai; Schu-Rern Chern; Chen-Chi Lee; Wayseen Wang
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.
European journal of medical genetics 2008;51(4):368-72.
2008: Chih-Ping Chen; Shuan-Pei Lin; Fuu-Jen Tsai; Schu-Rern Chern; Wayseen Wang
Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation.
Fertility and sterility 2008;89(6):1826.e5-7.
2008: Chih-Ping Chen; Tung-Yao Chang; Yu-Peng Liu; Fuu-Jen Tsai; Shu-Chin Chien; Chien-Ming Tsao; Hsiao-Bai Yang; Wayseen Wang
Prenatal 3-dimensional sonographic and MRI findings in omphalocele-exstrophy-imperforate anus-spinal defects complex.
Journal of clinical ultrasound : JCU 2008;36(5):308-11.
2008: 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
Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1-->pter) and partial trisomy 10q (10q25.1-->qter).
Prenatal diagnosis 2008;28(5):450-3.
2008: Chih-Ping Chen; Yann-Jang Chen; Fuu-Jen Tsai; Schu-Rern Chern; Wayseen Wang
NFkappaB2 gene duplication is associated with fetal pyelectasis in partial trisomy 10q (10q24.1 --> qter).
Prenatal diagnosis 2008;28(4):364-5.
2008: Chih-Ping Chen; Jin-Chung Shih; Chin-Yuan Tzen; Schu-Rern Chern; Chen-Ju Lin; Wayseen Wang
Prenatal visualization of cebocephaly with a prominent nose in a second-trimester fetus with alobar holoprosencephaly and trisomy 13.
Taiwanese journal of obstetrics & gynecology 2008;47(1):95-7.
2008: Chih-Ping Chen; Tung-Yao Chang; Hung-Hung Lin; Schu-Rern Chern; Wayseen Wang
Concomitant omphalocele and anencephaly associated with trisomy 18 and arthrogryposis diagnosed in early pregnancy.
Taiwanese journal of obstetrics & gynecology 2008;47(1):93-4.
2008: Chih-Ping Chen; Tung-Yao Chang; Jeng-Hsiu Hung; Chen-Yu Chen; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2008;47(1):91-2.
2008: Chih-Ping Chen; Shuan-Pei Lin; Y-N Su; S-C Chien; Fuu-Jen Tsai; Wayseen Wang
Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutation.
Genetic counseling (Geneva, Switzerland) 2008;19(2):165-72.
2007: Chih-Ping Chen; Tung-Yao Chang; Wayseen Wang
Third-trimester ultrasound evaluation of arachnoid cysts.
Taiwanese journal of obstetrics & gynecology 2007;46(4):427-8.
2007: Chih-Ping Chen; Fuu-Jen Tsai; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town; Wayseen Wang
Cytogenetic variability in the proportion of abnormal cells between the various tissues in prenatally detected mosaic tetrasomy 12p.
Prenatal diagnosis 2007;27(12):1170-3.
2007: Chih-Ping Chen; Tzu-Hao Wang; Yann-Jang Chen; Tung-Yao Chang; Yu-Peng Liu; Chin-Yuan Tzen; Schu-Rern Chern; Wayseen Wang
Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1.
Prenatal diagnosis 2007;27(10):967-9.
2007: Hsiao-En Cindy Chen; Chih-Ping Chen; Chin-Yuan Hsu; Wayseen Wang
Typical body wall defect associated with craniofacial anomalies and amniotic bands diagnosed in early pregnancy.
Taiwanese journal of obstetrics & gynecology 2007;46(3):286-7.
2007: Chih-Ping Chen; Tung-Yao Chang; Yu-Peng Liu; Schu-Rern Chern; Wayseen Wang
Prenatal magnetic resonance imaging evaluation of a digynic triploid fetus.
Taiwanese journal of obstetrics & gynecology 2007;46(3):284-5.
2007: Chih-Ping Chen; Tung-Yao Chang; Schu-Rern Chern; Wayseen Wang
Third-trimester 3D ultrasound evaluation of thanatophoric dysplasia type I.
Taiwanese journal of obstetrics & gynecology 2007;46(3):281-3.
2007: Chih-Ping Chen; Shuan-Pei Lin; Tung-Yao Chang; Hung-Chang Lee; Han-Yang Hung; Hsiang-Yu Lin; Jian-Pei Huang; Wayseen Wang
Prenatal sonographic findings of Klippel-Trénaunay-Weber syndrome.
Journal of clinical ultrasound : JCU 2007;35(7):409-12.
2007: Chih-Ping Chen; Chin-Yuan Hsu; Chin-Yuan Tzen; Chen-Chi Lee; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang
Prenatal diagnosis of mosaic ring chromosome 4.
Prenatal diagnosis 2007;27(5):485-7.
2007: Chih-Ping Chen; Tung-Yao Chang; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town; Meng-Shan Lee; Wayseen Wang
Prenatal diagnosis of low-level mosaic tetrasomy 9p by amniocentesis.
Prenatal diagnosis 2007;27(4):383-5.
2007: Chih-Ping Chen; Yu-Peng Liu; Shu-Chin Chien; Wayseen Wang
Prenatal diagnosis of concomitant gallbladder hydrops and pyelectasis with spontaneous resolution.
Taiwanese journal of obstetrics & gynecology 2007;46(1):81-2.
2007: Chih-Ping Chen; Chen-Ju Lin; Tung-Yao Chang; Schu-Rern Chern; Chin-Yuan Tzen; Wen-Lin Chen; Wayseen Wang
Prenatal diagnosis of the hypoplastic right heart syndrome with sex chromosome pentasomy (49,XXXXY).
Prenatal diagnosis 2007;27(3):285-6.
2007: Chih-Ping Chen; S C Chien; Schu-Rern Chern; Chin-Yuan Tzen; Wayseen Wang
Prenatal diagnosis of Dandy-Walker malformation associated with distal limb deficiencies.
Genetic counseling (Geneva, Switzerland) 2007;18(3):343-7.
2007: Chih-Ping Chen; Chen-Ju Lin; Tung-Yao Chang; Chin-Yuan Hsu; Chin-Yuan Tzen; Wayseen Wang
Second-trimester diagnosis of limb-body wall complex with literature review of pathogenesis.
Genetic counseling (Geneva, Switzerland) 2007;18(1):105-12.
2007: Chih-Ping Chen; Shuan-Pei Lin; Chin-Yuan Tzen; W L Hwu; Schu-Rern Chern; Chih-Kuang Chuang; S S Chiang; Wayseen Wang
Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome).
Genetic counseling (Geneva, Switzerland) 2007;18(1):49-56.
2007: Chih-Ping Chen; Chin-Yuan Hsu; Chin-Yuan Tzen; Schu-Rern Chern; Wayseen Wang
Prenatal diagnosis of pentalogy of Cantrell associated with hypoplasia of the right upper limb and ectrodactyly.
Prenatal diagnosis 2007;27(1):86-7.
2006: Chih-Ping Chen; Schu-Rern Chern; Pei-Yin Lee; Dai-Dyi Town; Wayseen Wang
Prenatal diagnosis of low-level mosaic trisomy 6 by amniocentesis.
Prenatal diagnosis 2006;26(11):1093-6.
2006: Chih-Ping Chen; Chyi-Chyang Lin; Yueh-Chun Li; Lie-Jiau Hsieh; Chen-Chi Lee; Wayseen Wang
Primary ovarian failure in a mentally retarded woman with a de novo unbalanced X;autosome translocation.
Fertility and sterility 2006;86(5):1514.e1-2.
2006: Chih-Ping Chen; Tzu-Hao Wang; Shuan-Pei Lin; Schu-Rern Chern; M-R Chen; Chen-Chi Lee; Yann-Jang Chen; Wayseen Wang
24 Mb deletion of 6q22.1-->q23.2 in an infant with pulmonary atresia, ventricular septal defect, microcephaly, developmental delay and facial dysmorphism.
European journal of medical genetics 2006;49(6):516-9.
2006: Chih-Ping Chen; Chen-Li Lin; Li-Lu Chen; Chen-Chi Lee; Wayseen Wang
Prenatal diagnosis of mosaic ring chromosome 9.
Prenatal diagnosis 2006;26(9):870-1.
2006: Chih-Ping Chen; Shuan-Pei Lin; Tzu-Hao Wang; Yann-Jang Chen; Ming Chen; Wayseen Wang
Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3-->q31.3) associated with Gorlin syndrome.
Prenatal diagnosis 2006;26(8):725-9.
2006: Chih-Ping Chen; Chyi-Chyang Lin; Tung-Yao Chang; Yueh-Chun Li; Lie-Jiau Hsieh; Chen-Chi Lee; Li-Feng Chen; Wayseen Wang
Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->ter-->qter).
Prenatal diagnosis 2006;26(8):757-9.
2006: Chih-Ping Chen; Tzu-Hao Wang; Schu-Rern Chern; Chin-Yuan Tzen; Chin-Yuan Hsu; Chen-Chi Lee; Li-Feng Chen; Chung-Chun Ma; Po-Tsang Chen; Wayseen Wang
Prenatal diagnosis of congenital chylothorax associated with de novopartial trisomy 12q (12q21.2-->qter).
Prenatal diagnosis 2006;26(8):752-5.
2006: Chih-Ping Chen; Shuan-Pei Lin; Chyi-Chyang Lin; Yann-Jang Chen; Schu-Rern Chern; Yueh-Chun Li; Lie-Jiau Hsieh; Chen-Chi Lee; Chen-Wen Pan; Wayseen Wang
Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q.
American journal of medical genetics. Part A 2006;140(14):1594-600.
2006: Chih-Ping Chen; Yi-Ning Su; Chia-Cheng Hung; Jin-Chung Shih; Wayseen Wang
Novel mutation in the TSC2 gene associated with prenatally diagnosed cardiac rhabdomyomas and cerebral tuberous sclerosis.
Journal of the Formosan Medical Association = Taiwan yi zhi 2006;105(7):599-603.
2006: Chih-Ping Chen; Yu-Peng Liu; Chin-Yuan Hsu; Shuan-Pei Lin; Wayseen Wang
Prenatal sonography and magnetic resonance imaging of pulmonary sequestration associated with a gastric duplication cyst.
Prenatal diagnosis 2006;26(5):489-91.
2006: Chih-Ping Chen; Shuan-Pei Lin; Chyi-Chyang Lin; Yueh-Chun Li; Lie-Jiau Hsieh; Schu-Rern Chern; Chen-Chi Lee; Li-Feng Chen; Hui-Min Hua; Wayseen Wang
Prenatal diagnosis of low-level mosaicism for a small XIST-negative supernumerary ring X chromosome in a nondysmorphic male fetus.
Prenatal diagnosis 2006;26(4):387-91.
2006: Chih-Ping Chen; Schu-Rern Chern; Chyi-Chyang Lin; Tzu-Hao Wang; Yueh-Chun Li; Lie-Jiau Hsieh; Chen-Chi Lee; Hui-Min Hua; Wayseen Wang
Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
Prenatal diagnosis 2006;26(4):313-20.
2006: C-P Chen; Shuan-Pei Lin; Y-N Su; J-K Huang; Wayseen Wang
A cloverleaf skull associated with Crouzon syndrome.
Archives of disease in childhood. Fetal and neonatal edition 2006;91(2):F98.
2006: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Chyi-Chyang Lin; Yueh-Chun Li; Lie-Jiau Hsieh; Wen-Lin Chen; Wayseen Wang
Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
Prenatal diagnosis 2006;26(2):138-46.
2006: Chih-Ping Chen; Yi-Ning Su; Shuan-Pei Lin; Mei-Ling Lin; Wayseen Wang
Favourable outcome in a pregnancy with concomitant maternal and fetal osteogenesis imperfecta associated with a novel COL1A2 mutation.
Prenatal diagnosis 2006;26(2):188-90.
2006: Chih-Ping Chen; Shuan-Pei Lin; Jin-Chern Sheu; Wayseen Wang; Chi-Yuan Tzen
Neonatal outcome of a prenatally detected 46,XX/46,XY true hermaphrodite.
Prenatal diagnosis 2006;26(2):185-6.
2006: Chih-Ping Chen; Schu-Rern Chern; Fang-Yu Hung; Chin-Yuan Hsu; Tung-Yao Chang; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Li-Feng Chen; Chin-Yuan Tzen; Wayseen Wang; Ryan Ma
Prenatal diagnosis of pure distal 18q deletion.
Prenatal diagnosis 2006;26(2):184-5.
2006: Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Chyi-Chyang Lin; Yueh-Chun Li; Chen-Chi Lee; Lie-Jiau Hsieh; Wen-Lin Chen; Wayseen Wang
Molecular cytogenetic analysis of de novo dup(5)(q33.1q31.1) associated with abnormal perinatal findings.
Prenatal diagnosis 2006;26(2):181-3.
2006: Chih-Ping Chen; Shuan-Pei Lin; Chen-Chi Lee; Dai-Dyi Town; Wayseen Wang
Partial trisomy 1p (1p36.22-->pter) and partial monosomy 9p (9p22.2-->pter) associated with achalasia, flexion deformity of the fingers and epilepsy in a girl.
Genetic counseling (Geneva, Switzerland) 2006;17(3):301-6.
2006: Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Chen-Chi Lee; Jon-Kway Huang; Wayseen Wang
Direct transmission of the 18q- syndrome from mother to daughter.
Genetic counseling (Geneva, Switzerland) 2006;17(2):185-9.
2006: Chih-Ping Chen; Tung-Yao Chang; Yi-Ning Su; Chin-Yuan Hsu; Wayseen Wang
Prenatal two- and three-dimensional ultrasound diagnosis of limb reduction defects associated with homozygous alpha-thalassemia.
Fetal diagnosis and therapy 2006;21(4):374-9.
2006: Chih-Ping Chen; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Li-Feng Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang
Detection of euchromatic variants and unusual C band heterochromatin variants at genetic amniocentesis.
Genetic counseling (Geneva, Switzerland) 2006;17(1):91-5.
2006: Chih-Ping Chen; Shuan-Pei Lin; Chyi-Chyang Lin; Yueh-Chun Li; Lie-Jiau Hsieh; Jon-Kway Huang; Chen-Chi Lee; Wayseen Wang
Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
Genetic counseling (Geneva, Switzerland) 2006;17(1):57-63.
2005: Chih-Ping Chen; Shuan-Pei Lin; Chyi-Chyang Lin; Yueh-Chun Li; Lie-Jiau Hsieh; Schu-Rern Chern; Chen-Chi Lee; Yen-Jiun Chen; Wayseen Wang
Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter).
Prenatal diagnosis 2005;25(12):1170-2.
2005: Chih-Ping Chen; Schu-Rern Chern; Shuan-Pei Lin; Chyi-Chyang Lin; Yueh-Chun Li; Tzu-Hao Wang; Chen-Chi Lee; Chen-Wen Pan; Lie-Jiau Hsieh; Wayseen Wang
A paternally derived inverted duplication of distal 14q with a terminal 14q deletion.
American journal of medical genetics. Part A 2005;139A(2):146-50.
2005: Chih-Ping Chen; Schu-Rern Chern; Tung-Yao Chang; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang
Prenatal diagnosis of partial trisomy 10q (10q25.3-->qter) and partial monosomy 18q (18q23-->qter).
Prenatal diagnosis 2005;25(11):1069-71.
2005: Chih-Ping Chen; Schu-Rern Chern; Li-Feng Chen; Wen-Lin Chen; Wayseen Wang
Prenatal diagnosis of low-level mosaic trisomy 7 by amniocentesis.
Prenatal diagnosis 2005;25(11):1067-9.
2005: Chih-Ping Chen; Chin-Yuan Hsu; Jon-Kway Huang; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang
Prenatal diagnosis of partial trisomy 16q and distal 22q13 deletion associated with dolichocephaly and frontal bossing on second-trimester ultrasound.
Prenatal diagnosis 2005;25(10):964-6.
2005: Chih-Ping Chen; Shuan-Pei Lin; Chyi-Chyang Lin; Yueh-Chun Li; Lie-Jiau Hsieh; Chen-Chi Lee; Yen-Jiun Chen; Wayseen Wang
Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial duplication of Yq (Yq11.2-->qter) and partial monosomy 5p (5p15.3-->pter).
Prenatal diagnosis 2005;25(8):723-5.
2005: Chih-Ping Chen; Yu-Peng Liu; Shuan-Pei Lin; Jin-Cherng Sheu; Chin-Yuan Hsu; Tung-Yao Chang; Wayseen Wang
Prenatal magnetic resonance imaging demonstration of the systemic feeding artery of a pulmonary sequestration associated with in utero regression.
Prenatal diagnosis 2005;25(8):721-3.
2005: Chih-Ping Chen; Jin-Chung Shih; Chin-Yuan Hsu; Chen-Yu Chen; Jon-Kway Huang; Wayseen Wang
Prenatal three-dimensional/four-dimensional sonographic demonstration of facial dysmorphisms associated with holoprosencephaly.
Journal of clinical ultrasound : JCU 2005;33(6):312-8.
2005: Chih-Ping Chen; Jin-Chung Shih; Tung-Yao Chang; Schu-Rern Chern; Ching-Yi Lin; Wayseen Wang; Chin-Yuan Tzen
Prenatal diagnosis of an acardiac amorphous twin and the anomalous co-twin in a monoamniotic twin pregnancy.
Prenatal diagnosis 2005;25(7):618-20.
2005: Chih-Ping Chen; Shojen Cheng; Yi-Hui Lin; Wayseen Wang
Prenatal imaging of limb-body wall complex by magnetic resonance imaging.
Prenatal diagnosis 2005;25(6):521-3.
2005: Chih-Ping Chen; Tung-Yao Chang; Shuan-Pei Lin; Jon-Kway Huang; Jeng-Daw Tsai; Nan-Chang Chiu; Wayseen Wang
Prenatal magnetic resonance imaging of Galloway-Mowat syndrome.
Prenatal diagnosis 2005;25(6):525-7.
2005: Chih-Ping Chen; Yu-Peng Liu; Jon-Kway Huang; Tung-Yao Chang; Ming-Ren Chen; Nan-Chang Chiu; Wayseen Wang
Contribution of ultrafast magnetic resonance imaging in prenatal diagnosis of sonographically undetected cerebral tuberous sclerosis associated with cardiac rhabdomyomas.
Prenatal diagnosis 2005;25(6):523-4.
2005: Chih-Ping Chen; Schu-Rern Chern; Jin-Chern Sheu; Shuan-Pei Lin; Chin-Yuan Hsu; Tung-Yao Chang; Chen-Chi Lee; Wayseen Wang; Hsiao-En Cindy Chen
Prenatal diagnosis, sonographic findings and molecular genetic analysis of a 46,XX/46,XY true hermaphrodite chimera.
Prenatal diagnosis 2005;25(6):502-6.
2005: Chih-Ping Chen; Schu-Rern Chern; Tzu-Hao Wang; Ding-Wei Hsueh; Chen-Chi Lee; Dai-Dyi Town; Wayseen Wang; Tsang-Ming Ko
Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
Prenatal diagnosis 2005;25(6):492-6.
2005: Chih-Ping Chen; Shuan-Pei Lin; Chen-Chi Lee; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang
Perinatal findings of partial trisomy 13q (13q14.1-->qter) resulting from paternal pericentric inversion of chromosome 13.
Prenatal diagnosis 2005;25(6):527-8.
2005: Chih-Ping Chen; Schu-Rern Chern; Tung-Yao Chang; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang; Hsiao-En Cindy Chen
Prenatal diagnosis of de novo proximal interstitial deletion of 9q and review of the literature of uncommon aneuploidies associated with increased nuchal translucency.
Prenatal diagnosis 2005;25(5):383-9.
2005: Chih-Ping Chen; Jin-Chung Shih; Chin-Yuan Tzen; Yi-Hui Lin; Wayseen Wang
Recurrent short-rib polydactyly syndrome: prenatal three-dimensional ultrasound findings and associations with congenital high airway obstruction and pyelectasia.
Prenatal diagnosis 2005;25(5):417-8.
2005: Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Ching-Yi Lin; Yi-Hui Lin; Wayseen Wang
A comparison of maternal age, sex ratio and associated major anomalies among fetal trisomy 18 cases with different cell division of error.
Prenatal diagnosis 2005;25(4):327-30.
2005: Chih-Ping Chen; Schu-Rern Chern; Chin-Yuan Hsu; Chen-Chi Lee; Meng-Shan Lee; Wayseen Wang
Prenatal diagnosis of de novo partial trisomy 13q (13q22 --> qter) and partial monosomy 8p (8p23.3 --> pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart.
Prenatal diagnosis 2005;25(4):334-6.
2005: Chih-Ping Chen; Chen-Yu Chen; Ching-Yi Lin; Sheng-Wen Shaw; Wayseen Wang; Chin-Yuan Tzen
Prenatal diagnosis of concomitant alobar holoprosencephaly and caudal regression syndrome associated with maternal diabetes.
Prenatal diagnosis 2005;25(3):264-6.
2005: Chih-Ping Chen; Tung-Yao Chang; Chin-Yuan Tzen; Wayseen Wang; Chen-Chi Lee
Recurrent fetal pyelectasis in a family with fetuses associated with partial trisomy 10q (10q24.1-->qter).
Prenatal diagnosis 2005;25(3):263-4.
2005: Chih-Ping Chen; Yi-Ning Su; Jian-Pei Huang; Yi-Hui Lin; Wayseen Wang
Asymmetrical terminal limb defects in a hydropic infant with homozygous alpha-thalassemia-1.
Prenatal diagnosis 2005;25(2):178-9.
2005: Chih-Ping Chen; Shuan-Pei Lin; Chyi-Chyang Lin; Yueh-Chun Li; Schu-Rern Chern; Wei-Min Chen; Chen-Chi Lee; Lie-Jiau Hsieh; Wayseen Wang
Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).
Prenatal diagnosis 2005;25(2):112-8.
2005: Chih-Ping Chen; Yi-Ning Su; Chia-Cheng Hung; Chien-Nan Lee; Fon-Jou Hsieh; Tung-Yao Chang; Ming-Ren Chen; Wayseen Wang
Molecular genetic analysis of the TSC genes in two families with prenatally diagnosed rhabdomyomas.
Prenatal diagnosis 2005;25(2):176-8.
2005: Chih-Ping Chen; Schu-Rern Chern; Chen-Ju Lin; Chen-Chi Lee; Wayseen Wang; Chin-Yuan Tzen
A comparison of maternal age, sex ratio and associated anomalies among numerically aneuploid, structurally aneuploid and euploid holoprosencephaly.
Genetic counseling (Geneva, Switzerland) 2005;16(1):49-57.
2004: Chih-Ping Chen; Jin-Chern Sheu; Jon-Kway Huang; Yi-Hui Lin; Chin-Yuan Tzen; Wayseen Wang
Second-trimester magnetic resonance imaging of fetal sacrococcygeal teratoma with intrapelvic extension in a co-twin.
Prenatal diagnosis 2004;24(12):1015-7.
2004: Chih-Ping Chen; Chen-Chi Lee; Wayseen Wang
Prenatal diagnosis of complete trisomy 16q in two consecutive pregnancies.
Prenatal diagnosis 2004;24(12):1019-20.
2004: Chih-Ping Chen; Chen-Chi Lee; Wayseen Wang
Prenatal diagnosis of complete trisomy 16q in two consecutive pregnancies.
Prenatal diagnosis 2004;24(11):928-9.
2004: Chih-Ping Chen; Chin-Yuan Hsu; Chen-Chi Lee; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang
Prenatal diagnosis of de novo pure partial monosomy 4p (4p15.1-->pter) in a growth-restricted fetus with a Greek warrior helmet face and unilateral facial cleft on three-dimensional ultrasound.
Prenatal diagnosis 2004;24(11):934-6.
2004: Chih-Ping Chen; Chyi-Chyang Lin; Yueh-Chun Li; Schu-Rern Chern; Chen-Chi Lee; Wen-Lin Chen; Men-Shan Lee; Wayseen Wang; Chin-Yuan Tzen
Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature.
Prenatal diagnosis 2004;24(10):767-73.
2004: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Shuan-Pei Lin; Tung-Yao Chang; Wayseen Wang
Prenatal diagnosis of mosaic 22q11.2 microdeletion.
Prenatal diagnosis 2004;24(8):660-2.
2004: Chih-Ping Chen; Schu-Rern Chern; Shojen Cheng; Tung-Yao Chang; Li-Fan Yeh; Chen-Chi Lee; Chen-Wen Pan; Wayseen Wang; Chin-Yuan Tzen
Second-trimester diagnosis of complete trisomy 9 associated with abnormal maternal serum screen results, open sacral spina bifida and congenital diaphragmatic hernia, and review of the literature.
Prenatal diagnosis 2004;24(6):455-62.
2004: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang
Prenatal diagnosis of interstitially satellited 6p.
Prenatal diagnosis 2004;24(6):430-3.
2004: Chih-Ping Chen; Tung-Yao Chang; Yi-Hui Lin; Wayseen Wang
Prenatal sonographic diagnosis of acrania associated with amniotic bands.
Journal of clinical ultrasound : JCU 2004;32(5):256-60.
2004: Chih-Ping Chen; Han-Yang Hung; Tung-Yao Chang; Shuan-Pei Lin; Wayseen Wang
Second-trimester nasal bone hypoplasia/aplasia associated with cleidocranial dysplasia.
Prenatal diagnosis 2004;24(5):399-400.
2004: Chih-Ping Chen; Shuan-Pei Lin; Yuh-Ming Hwu; Tung-Yao Chang; Wayseen Wang
Prenatal identification of fetal overgrowth, abdominal wall defect, and neural tube defect in pregnancies achieved by assisted reproductive technology.
Prenatal diagnosis 2004;24(5):396-8.
2004: Chih-Ping Chen; Shuan-Pei Lin; Chin-Yuan Tzen; Fuu-Jen Tsai; Wuh-Liang Hwu; Wayseen Wang
Detection of a homozygous D645E mutation of the acid alpha-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II.
Prenatal diagnosis 2004;24(3):231-2.
2004: Chih-Ping Chen; Schu-Rern Chern; Tung-Yao Chang; Chin-Yuan Tzen; Chen-Chi Lee; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang
Prenatal diagnosis of the distal 11q deletion and review of the literature.
Prenatal diagnosis 2004;24(2):130-6.
2004: Chih-Ping Chen; Tung-Yao Chang; Dai-Dyi Town; Li-Feng Chen; Chen-Wen Pan; Wayseen Wang; Chin-Yuan Tzen
Partial trisomy 10 (10q11.2-->pter) and partial trisomy 18 (18p11.2-->pter) associated with abnormal sonographic findings and a maternal serum screen-positive result.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2004;23(2):202-4.
2004: Chih-Ping Chen; Chen-Chi Lee; Dai-Dyi Town; Meng-Shan Lee; Wayseen Wang
Discrepancy between the fetus and extra-embryonic tissues in prenatally detected mosaic distal 5p deletion.
Genetic counseling (Geneva, Switzerland) 2004;15(4):473-6.
2004: Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Chen-Chi Lee; Jon-Kway Huang; Wayseen Wang; You-Wei Liao
De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delay.
Genetic counseling (Geneva, Switzerland) 2004;15(4):437-42.
2004: Chih-Ping Chen; Shojen Cheng; Tung-Yao Chang; Li-Fan Yeh; Yi-Hui Lin; Wayseen Wang
Prenatal diagnosis of choledochal cyst using ultrasound and magnetic resonance imaging.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2004;23(1):93-4.
2004: Chih-Ping Chen; Jin-Chung Shih; Schu-Rern Chern; Chen-Chi Lee; Wayseen Wang
Prenatal diagnosis of mosaic trisomy 16 associated with congenital diaphragmatic hernia and elevated maternal serum alpha-fetoprotein and human chorionic gonadotrophin.
Prenatal diagnosis 2004;24(1):63-6.
2004: Chih-Ping Chen; Chen-Chi Lee; Tung-Yao Chang; Dai-Dyi Town; Wayseen Wang
Prenatal diagnosis of mosaic distal 5p deletion and review of the literature.
Prenatal diagnosis 2004;24(1):50-7.
2004: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Tung-Yao Chang; Wayseen Wang; Chin-Yuan Tzen
Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.
Prenatal diagnosis 2004;24(1):38-44.
2004: Chih-Ping Chen; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang; Chin-Yuan Tzen
Prenatal diagnosis of premature centromere division-related mosaic variegated aneuploidy.
Prenatal diagnosis 2004;24(1):19-25.
2003: Chih-Ping Chen; Schu-Rern Chern; Dai-Dyi Town; Wayseen Wang; You-Wei Liao
Fetoplacental and fetoamniotic chromosomal discrepancies in prenatally detected mosaic trisomy 9.
Prenatal diagnosis 2003;23(12):1019-21.
2003: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Li-Feng Chen; Daniel T H Chin; Chin-Yuan Tzen; Wayseen Wang
Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion.
Prenatal diagnosis 2003;23(9):758-61.
2003: Chih-Ping Chen; J-C Shih; Shin-Lin Shih; J-K Huang; J-P Huang; Y-H Lin; Wayseen Wang
Prenatal diagnosis of cephalothoracopagus janiceps disymmetros using three-dimensional power Doppler ultrasound and magnetic resonance imaging.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2003;22(3):299-304.
2003: Chih-Ping Chen; Jin-Chung Shih; Jon-Kway Huang; Wayseen Wang; Chin-Yuan Tzen
Second-trimester evaluation of fetal sacrococcygeal teratoma using three-dimensional color Doppler ultrasound and magnetic resonance imaging.
Prenatal diagnosis 2003;23(7):602-3.
2003: Chih-Ping Chen; Chyong-Hsin Hsu; Shuan-Pei Lin; Che-Sheng Ho; Chen-Chi Lee; Wayseen Wang
Association of partial trisomy 9 (9pter-->q22.3) with corpus callosum dysgenesis, bilateral subependymal cysts, and ventriculomegaly.
Prenatal diagnosis 2003;23(6):519-20.
2003: Chih-Ping Chen; Jin-Chung Shih; Jui-Hsing Chang; Yi-Hui Lin; Wayseen Wang
Prenatal diagnosis of right pulmonary agenesis associated with VACTERL sequence.
Prenatal diagnosis 2003;23(6):515-8.
2003: Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Shin-Lin Shih; Chen-Chi Lee; Wayseen Wang; You-Wei Liao
Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion.
Prenatal diagnosis 2003;23(6):504-8.
2003: Chih-Ping Chen; Tung-Yao Chang; Chin-Yuan Tzen; Wayseen Wang; Chen-Chi Lee; Li-Feng Chen; Meng-Shan Lee; Shaun-Pei Lin
Second-trimester sonographic demonstration of retrognathia and bilateral pyelectasis in a fetus with a duplication of chromosome 10q24.1-->qter.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2003;21(5):516-8.
2003: Chih-Ping Chen; Schu-Rern Chern; Tung-Yao Chang; Chin-Yuan Tzen; Chen-Chi Lee; Wen-Lin Chen; Meng-Shan Lee; Wayseen Wang
Prenatal diagnosis of de novo terminal deletion of chromosome 7q.
Prenatal diagnosis 2003;23(5):375-9.
2003: Chih-Ping Chen; Yuh-Ming Hwu; Li-Fan Yeh; Schu-Rern Chern; Chen-Chi Lee; Wayseen Wang
Successful triplet pregnancy and delivery after oocyte donation in an infertile female with chromosome mosaicism for monosomy X, partial trisomy X, and terminal Xp deletion.
Fertility and sterility 2003;79(5):1231-3.
2003: Chih-Ping Chen; Tung-Yao Chang; Chin-Yuan Tzen; Wayseen Wang
Second-trimester sonographic detection of short rib-polydactyly syndrome type II (Majewski) following an abnormal maternal serum biochemical screening result.
Prenatal diagnosis 2003;23(4):353-5.
2003: Chih-Ping Chen; Tung-Yao Chang; Schu-Rern Chern; Dai-Dyi Town; Chen-Wen Pan; Meng-Shan Lee; Wayseen Wang
Early second-trimester diagnosis of monozygotic twins discordant for cystic hygroma colli and Turner syndrome.
Prenatal diagnosis 2003;23(4):352-3.
2003: Chih-Ping Chen; Schu-Rern Chern; Shuan-Pei Lin; Wayseen Wang; Fuu-Jen Tsai
Prenatal identification of a G338E mutation in FGFR2 in a fetus without sonographic appearance of craniosynostosis.
Prenatal diagnosis 2003;23(2):175-6.
2003: Chih-Ping Chen; Schu-Rern Chern; Tung-Yao Chang; Chen-Chi Lee; Li-Feng Chen; Chin-Yuan Tzen; Wayseen Wang; Chen-Ju Lin; Brian P T Yang; Lawrence S T Yang
Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction.
Prenatal diagnosis 2003;23(1):40-3.
2002: Chih-Ping Chen; Chin-Yuan Tzen; Tung-Yao Chang; Chen-Ju Lin; Wayseen Wang; Chen-Chi Lee; Dai-Dyi Town; Li-Feng Chen; Meng-Shan Lee
Prenatal diagnosis of partial trisomy 3p and partial monosomy 11q in a fetus with a Dandy-Walker variant and trigonocephaly.
Prenatal diagnosis 2002;22(12):1112-3.
2002: Chih-Ping Chen; Tung-Yao Chang; Jin-Chung Shih; Shuan-Pei Lin; Chen-Ju Lin; Wayseen Wang; Chen-Chi Lee; Dai-Dyi Town; Chen-Wen Pan; Chin-Yuan Tzen
Prenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion.
Prenatal diagnosis 2002;22(12):1063-6.
2002: Chih-Ping Chen; Shuan-Pei Lin; Tung-Yao Chang; Nan-Chang Chiu; Shin-Lin Shih; Chen-Ju Lin; Wayseen Wang; Hong-Chih Hsu
Perinatal imaging findings of inherited Sotos syndrome.
Prenatal diagnosis 2002;22(10):887-92.
2002: Chih-Ping Chen; Schu-Rern Chern; Tung-Yao Chang; Chen-Ju Lin; Wayseen Wang; Chin-Yuan Tzen
Second trimester molecular diagnosis of a stop codon FGFR3 mutation in a type I thanatophoric dysplasia fetus following abnormal ultrasound findings.
Prenatal diagnosis 2002;22(8):736-7.
2002: Chih-Ping Chen; Chin-Yuan Tzen; Tung-Yao Chang; Li-Fan Yeh; Wayseen Wang
Prenatal diagnosis of acrania associated with facial defects, amniotic bands and limb-body wall complex.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2002;20(1):94-5.
2002: Chih-Ping Chen; Yuh-Cheng Yang; Shuan-Pei Lin; Wayseen Wang; Chih-Long Chang; Kuo-Ming Chang
Bilateral calcified ovarian fibromas in a patient with Sotos syndrome.
Fertility and sterility 2002;77(6):1285-7.
2002: Chih-Ping Chen; Tung-Yao Chang; Li-Fan Yeh; Chen-Ju Lin; Wayseen Wang
Sonographic appearance of the uterus after simple square suturing for rapid control of postpartum hemorrhage and preservation of fertility.
Journal of clinical ultrasound : JCU 2002;30(3):189-91.
2002: Chih-Ping Chen; Jin-Cherng Sheu; Wayseen Wang; Shuan-Pei Lin; Tung-Yao Chang; Chin-Yuan Tzen
Fetal cervico-mediastinal cystic hygroma associated with maternal serum screening positive for Down syndrome.
Prenatal diagnosis 2002;22(2):166.
2002: Chih-Ping Chen; Schu-Rern Chern; Shin-Hua Du; Wayseen Wang
Molecular diagnosis of a novel heterozygous 268C-->T (R90C) mutation in TGIF gene in a fetus with holoprosencephaly and premaxillary agenesis.
Prenatal diagnosis 2002;22(1):5-7.
2001: Chih-Ping Chen; Schu-Rern Chern; Wayseen Wang; Chen-Chi Lee; Wen-Lin Chen; Li-Feng Chen; Tung-Yao Chang; Chin-Yuan Tzen
Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
Prenatal diagnosis 2001;21(5):346-50.
2001: C P Chen; S R Chern; Wayseen Wang
Fetal DNA analyzed in plasma from a mother's three consecutive pregnancies to detect paternally inherited aneuploidy.
Clinical chemistry 2001;47(5):937-9.
2001: Chih-Ping Chen; Schu-Rern Chern; Chin-Yuan Tzen; Meng-Shan Lee; Chen-Wen Pan; Tung-Yao Chang; Wayseen Wang
Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial clefts.
Prenatal diagnosis 2001;21(4):317-20.
2001: Chih-Ping Chen; Schu-Rern Chern; Wayseen Wang; K L Wang; Tao-Yeuan Wang
Multiple globules in a cystic ovarian teratoma.
Fertility and sterility 2001;75(3):618-9.
2001: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang
Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly.
Prenatal diagnosis 2001;21(2):102-5.
2001: Chih-Ping Chen; Schu-Rern Chern; Jin-Chung Shih; Wayseen Wang; Li-Fan Yeh; Tung-Yao Chang; Chin-Yuan Tzen
Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasia.
Prenatal diagnosis 2001;21(2):89-95.
2000: Chih-Ping Chen; Schu-Rern Chern; C L Chang; Chen-Chi Lee; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang
Prenatal diagnosis and genetic analysis of X chromosome polysomy 49, XXXXY.
Prenatal diagnosis 2000;20(9):754-7.
2000: Chih-Ping Chen; Schu-Rern Chern; Li-Fan Yeh; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang
Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18.
Prenatal diagnosis 2000;20(9):750-3.
2000: Chih-Ping Chen; koenraad devriendt; Schu-Rern Chern; Chen-Chi Lee; Wayseen Wang; Shuan-Pei Lin
Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
Prenatal diagnosis 2000;20(5):384-9.
2000: Chih-Ping Chen; Schu-Rern Chern; Wayseen Wang
Rapid determination of zygosity and common aneuploidies from amniotic fluid cells using quantitative fluorescent polymerase chain reaction following genetic amniocentesis in multiple pregnancies.
Human reproduction (Oxford, England) 2000;15(4):929-34.
1999: Chih-Ping Chen; koenraad devriendt; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang; Tao-Yeuan Wang
Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
Prenatal diagnosis 1999;19(10):986-9.
1999: Chih-Ping Chen; Jin-Chung Shih; Chen-Chi Lee; Li-Feng Chen; Wayseen Wang; Tao-Yeuan Wang
Prenatal diagnosis of a fetus with distal 10q trisomy.
Prenatal diagnosis 1999;19(9):876-8.
1999: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Wayseen Wang
Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3:1 segregation of maternal reciprocal translocation t(13;16)(q12.3; p13.2).
Prenatal diagnosis 1999;19(8):783-6.
1999: Chih-Ping Chen; S R Chen; Tao-Yeuan Wang; Wayseen Wang; Yuh-Ming Hwu
A frame shift mutation in the DNA-binding domain of the androgen receptor gene associated with complete androgen insensitivity, persistent müllerian structures, and germ cell tumors in dysgenetic gonads.
Fertility and sterility 1999;72(1):170-3.
1999: Chih-Ping Chen; Schu-Rern Chern; Tao-Yeuan Wang; Wayseen Wang; Kung-Liahng Wang; CJ Jeng
Androgen receptor gene mutations in 46,XY females with germ cell tumours.
Human reproduction (Oxford, England) 1999;14(3):664-70.
1998: Chih-Ping Chen; Wayseen Wang; Shuan-Pei Lin; Jin-Cherng Sheu; J D Tsai
Perinatal findings in a male fetus with congenital megacystis and anorectal malformations.
Fetal diagnosis and therapy 1998;13(6):348-51.