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Wayseen Wang

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Physiology

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Newborn Infant

Anatomy

Chromosomes, Human, Pair 18

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Co-Publications
Name
78
Chen, Chih-Ping
72
Chern, Schu-Rern
51
Chang, Tung-Yao
42
Lee, Chen-Chi
40
Lin, Shuan-Pei
39
Tzen, Chin-Yuan
21
Tsai, Fuu-Jen
16
Town, Dai-Dyi
15
Chen, Wen-Lin
14
Lin, Chyi-Chyang
13
Hsieh, Lie-Jiau
11
Lee, Meng-Shan
9
Huang, Jon-Kway
9
Wang, Tzu-Hao
8
Pan, Chen-Wen

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Publications

TOP 3
Chen Chih-Ping; Su Yi-Ning; Chang Tung-Yao; Liu Yu-Peng; Tsai Fuu-Jen; Hwang Jonathan Kwei; Wang Wayseen
Prenatal magnetic resonance imaging, ultrasound imaging findings and genetic analysis of concomitant rhabdomyomas and cerebral tuberous sclerosis.
Chen Chih-Ping; Chern Schu-Rern; Tsai Fuu-Jen; Hsu Chin-Yuan; Ko Kevin; Wang Wayseen
Prenatal diagnosis and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly.
Chen Chih-Ping; Chern Schu-Rern; Tsai Fuu-Jen; Lin Hung-Hung; Pan Chen-Wen; Wang Wayseen
Prenatal diagnosis and molecular analysis of trisomy 13 mosaicism.

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All Publications

2009: Chen Chih-Ping; Su Yi-Ning; Chang Tung-Yao; Liu Yu-Peng; Tsai Fuu-Jen; Hwang Jonathan Kwei; Wang Wayseen
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: Chen Chih-Ping; Chern Schu-Rern; Tsai Fuu-Jen; Hsu Chin-Yuan; Ko Kevin; Wang Wayseen
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: Chen Chih-Ping; Chern Schu-Rern; Tsai Fuu-Jen; Lin Hung-Hung; Pan Chen-Wen; Wang Wayseen
Prenatal diagnosis and molecular analysis of trisomy 13 mosaicism.
Taiwanese journal of obstetrics & gynecology 2009;48(3):321-2.
2009: Chen Chih-Ping; Liu Yu-Peng; Tsai Fuu-Jen; Chen Chen-Yu; Lin Hung-Hung; Wu Pei-Chen; Wang Wayseen
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: Chen Chih-Ping; Tsai Fuu-Jen; Chern Schu-Rern; Chang Tung-Yao; Hsu Chin-Yuan; Lin Hung-Hung; Wang Wayseen
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: Chen Chih-Ping; Tzen Chin-Yuan; Chern Schu-Rern; Tsai Fuu-Jen; Hsu Chin-Yuan; Lee Chen-Chi; Lee Meng-Shan; Pan Chen-Wen; Wang Wayseen
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: Chen Chih-Ping; Tzen Chin-Yuan; Chen Chen-Yu; Tsai Fuu-Jen; Wang Wayseen
Concomitant exencephaly and limb defects associated with pentalogy of Cantrell.
Taiwanese journal of obstetrics & gynecology 2008;47(4):476-7.
2008: Chen Chih-Ping; Tsai Fuu-Jen; Chen Chen-Yu; Lin Hung-Hung; Wang Wayseen
Limb-body wall complex with craniofacial defects after ovarian stimulation.
Taiwanese journal of obstetrics & gynecology 2008;47(4):474-5.
2008: Chen Chih-Ping; Wang Tzu-Hao; Lin Chyi-Chyang; Tsai Fuu-Jen; Hsieh Lie-Jiau; Wang Wayseen
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: Chen Chih-Ping; Lin Shuan-Pei; Tsai Fuu-Jen; Wang Tzu-Hao; Chern Schu-Rern; Wang Wayseen
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: Chen Chih-Ping; Chen Yann-Jang; Chern Schu-Rern; Tsai Fuu-Jen; Lin Hung-Hung; Lee Chen-Chi; Wang Wayseen
Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele.
Prenatal diagnosis 2008;28(9):865-7.
2008: Chen Chih-Ping; Lin Shuan-Pei; Tsai Fuu-Jen; Chern Schu-Rern; Lee Chen-Chi; Wang Wayseen
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: Chen Chih-Ping; Lin Shuan-Pei; Tsai Fuu-Jen; Chern Schu-Rern; Wang Wayseen
Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctation.
Fertility and sterility 2008;89(6):1826.e5-7.
2008: Chen Chih-Ping; Chang Tung-Yao; Liu Yu-Peng; Tsai Fuu-Jen; Chien Shu-Chin; Tsao Chien-Ming; Yang Hsiao-Bai; Wang Wayseen
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: Chen Chih-Ping; Chen Yann-Jang; Chern Schu-Rern; Tsai Fuu-Jen; Chang Tung-Yao; Lee Chen-Chi; Town Dai-Dyi; Lee Meng-Shan; Wang Wayseen
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: Chen Chih-Ping; Chen Yann-Jang; Tsai Fuu-Jen; Chern Schu-Rern; Wang Wayseen
NFkappaB2 gene duplication is associated with fetal pyelectasis in partial trisomy 10q (10q24.1 --> qter).
Prenatal diagnosis 2008;28(4):364-5.
2008: Chen Chih-Ping; Shih Jin-Chung; Tzen Chin-Yuan; Chern Schu-Rern; Lin Chen-Ju; Wang Wayseen
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: Chen Chih-Ping; Chang Tung-Yao; Lin Hung-Hung; Chern Schu-Rern; Wang Wayseen
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: Chen Chih-Ping; Chang Tung-Yao; Hung Jeng-Hsiu; Chen Chen-Yu; Wang Wayseen
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: Chen C-P; Lin S-P; Su Y-N; Chien S-C; Tsai F-J; Wang W
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: Chen Chih-Ping; Chang Tung-Yao; Wang Wayseen
Third-trimester ultrasound evaluation of arachnoid cysts.
Taiwanese journal of obstetrics & gynecology 2007;46(4):427-8.
2007: Chen Chih-Ping; Tsai Fuu-Jen; Chern Schu-Rern; Lee Chen-Chi; Town Dai-Dyi; Wang Wayseen
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: Chen Chih-Ping; Wang Tzu-Hao; Chen Yann-Jang; Chang Tung-Yao; Liu Yu-Peng; Tzen Chin-Yuan; Chern Schu-Rern; Wang Wayseen
Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1.
Prenatal diagnosis 2007;27(10):967-9.
2007: Chen Hsiao-En Cindy; Chen Chih-Ping; Hsu Chin-Yuan; Wang Wayseen
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: Chen Chih-Ping; Chang Tung-Yao; Liu Yu-Peng; Chern Schu-Rern; Wang Wayseen
Prenatal magnetic resonance imaging evaluation of a digynic triploid fetus.
Taiwanese journal of obstetrics & gynecology 2007;46(3):284-5.
2007: Chen Chih-Ping; Chang Tung-Yao; Chern Schu-Rern; Wang Wayseen
Third-trimester 3D ultrasound evaluation of thanatophoric dysplasia type I.
Taiwanese journal of obstetrics & gynecology 2007;46(3):281-3.
2007: Chen Chih-Ping; Lin Shuan-Pei; Chang Tung-Yao; Lee Hung-Chang; Hung Han-Yang; Lin Hsiang-Yu; Huang Jian-Pei; Wang Wayseen
Prenatal sonographic findings of Klippel-Trénaunay-Weber syndrome.
Journal of clinical ultrasound : JCU 2007;35(7):409-12.
2007: Chen Chih-Ping; Hsu Chin-Yuan; Tzen Chin-Yuan; Lee Chen-Chi; Chen Wen-Lin; Chen Li-Feng; Wang Wayseen
Prenatal diagnosis of mosaic ring chromosome 4.
Prenatal diagnosis 2007;27(5):485-7.
2007: Chen Chih-Ping; Chang Tung-Yao; Chern Schu-Rern; Lee Chen-Chi; Town Dai-Dyi; Lee Meng-Shan; Wang Wayseen
Prenatal diagnosis of low-level mosaic tetrasomy 9p by amniocentesis.
Prenatal diagnosis 2007;27(4):383-5.
2007: Chen Chih-Ping; Liu Yu-Peng; Chien Shu-Chin; Wang Wayseen
Prenatal diagnosis of concomitant gallbladder hydrops and pyelectasis with spontaneous resolution.
Taiwanese journal of obstetrics & gynecology 2007;46(1):81-2.
2007: Chen Chih-Ping; Lin Chen-Ju; Chang Tung-Yao; Chern Schu-Rern; Tzen Chin-Yuan; Chen Wen-Lin; Wang Wayseen
Prenatal diagnosis of the hypoplastic right heart syndrome with sex chromosome pentasomy (49,XXXXY).
Prenatal diagnosis 2007;27(3):285-6.
2007: Chen Chih-Ping; Hsu Chin-Yuan; Tzen Chin-Yuan; Chern Schu-Rern; Wang Wayseen
Prenatal diagnosis of pentalogy of Cantrell associated with hypoplasia of the right upper limb and ectrodactyly.
Prenatal diagnosis 2007;27(1):86-7.
2007: Chen C P; Chien S C; Chern S R; Tzen C Y; Wang W
Prenatal diagnosis of Dandy-Walker malformation associated with distal limb deficiencies.
Genetic counseling (Geneva, Switzerland) 2007;18(3):343-7.
2007: Chen C P; Lin C J; Chang T Y; Hsu C Y; Tzen C Y; Wang W
Second-trimester diagnosis of limb-body wall complex with literature review of pathogenesis.
Genetic counseling (Geneva, Switzerland) 2007;18(1):105-12.
2007: Chen C P; Lin S P; Tzen C Y; Hwu W L; Chern S R; Chuang C K; Chiang S S; Wang W
Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome).
Genetic counseling (Geneva, Switzerland) 2007;18(1):49-56.
2006: Chen Chih-Ping; Chern Schu-Rern; Lee Pei-Yin; Town Dai-Dyi; Wang Wayseen
Prenatal diagnosis of low-level mosaic trisomy 6 by amniocentesis.
Prenatal diagnosis 2006;26(11):1093-6.
2006: Chen Chih-Ping; Lin Chyi-Chyang; Li Yueh-Chun; Hsieh Lie-Jiau; Lee Chen-Chi; Wang Wayseen
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: Chen C-P; Wang T-H; Lin S-P; Chern S-R; Chen M-R; Lee C-C; Chen Y-J; Wang W
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: Chen Chih-Ping; Lin Chen-Li; Chen Li-Lu; Lee Chen-Chi; Wang Wayseen
Prenatal diagnosis of mosaic ring chromosome 9.
Prenatal diagnosis 2006;26(9):870-1.
2006: Chen Chih-Ping; Lin Shuan-Pei; Wang Tzu-Hao; Chen Yann-Jang; Chen Ming; Wang Wayseen
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: Chen Chih-Ping; Lin Chyi-Chyang; Chang Tung-Yao; Li Yueh-Chun; Hsieh Lie-Jiau; Lee Chen-Chi; Chen Li-Feng; Wang Wayseen
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: Chen Chih-Ping; Wang Tzu-Hao; Chern Schu-Rern; Tzen Chin-Yuan; Hsu Chin-Yuan; Lee Chen-Chi; Chen Li-Feng; Ma Chung-Chun; Chen Po-Tsang; Wang Wayseen
Prenatal diagnosis of congenital chylothorax associated with de novopartial trisomy 12q (12q21.2-->qter).
Prenatal diagnosis 2006;26(8):752-5.
2006: Chen Chih-Ping; Su Yi-Ning; Hung Chia-Cheng; Shih Jin-Chung; Wang Wayseen
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: Chen Chih-Ping; Lin Shuan-Pei; Lin Chyi-Chyang; Chen Yann-Jang; Chern Schu-Rern; Li Yueh-Chun; Hsieh Lie-Jiau; Lee Chen-Chi; Pan Chen-Wen; Wang Wayseen
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: Chen Chih-Ping; Liu Yu-Peng; Hsu Chin-Yuan; Lin Shuan-Pei; Wang Wayseen
Prenatal sonography and magnetic resonance imaging of pulmonary sequestration associated with a gastric duplication cyst.
Prenatal diagnosis 2006;26(5):489-91.
2006: Chen Chih-Ping; Lin Shuan-Pei; Lin Chyi-Chyang; Li Yueh-Chun; Hsieh Lie-Jiau; Chern Schu-Rern; Lee Chen-Chi; Chen Li-Feng; Hua Hui-Min; Wang Wayseen
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: Chen Chih-Ping; Chern Schu-Rern; Lin Chyi-Chyang; Wang Tzu-Hao; Li Yueh-Chun; Hsieh Lie-Jiau; Lee Chen-Chi; Hua Hui-Min; Wang Wayseen
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: Chen C-P; Lin S-P; Su Y-N; Huang J-K; Wang W
A cloverleaf skull associated with Crouzon syndrome.
Archives of disease in childhood. Fetal and neonatal edition 2006;91(2):F98.
2006: Chen Chih-Ping; Chern Schu-Rern; Lee Chen-Chi; Lin Chyi-Chyang; Li Yueh-Chun; Hsieh Lie-Jiau; Chen Wen-Lin; Wang Wayseen
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: Chen Chih-Ping; Su Yi-Ning; Lin Shuan-Pei; Lin Mei-Ling; Wang Wayseen
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: Chen Chih-Ping; Lin Shuan-Pei; Sheu Jin-Chern; Wang Wayseen; Tzen Chi-Yuan
Neonatal outcome of a prenatally detected 46,XX/46,XY true hermaphrodite.
Prenatal diagnosis 2006;26(2):185-6.
2006: Chen Chih-Ping; Chern Schu-Rern; Hung Fang-Yu; Hsu Chin-Yuan; Chang Tung-Yao; Lee Chen-Chi; Town Dai-Dyi; Chen Wen-Lin; Chen Li-Feng; Tzen Chin-Yuan; Wang Wayseen; Ma Ryan
Prenatal diagnosis of pure distal 18q deletion.
Prenatal diagnosis 2006;26(2):184-5.
2006: Chen Chih-Ping; Lin Shuan-Pei; Chern Schu-Rern; Lin Chyi-Chyang; Li Yueh-Chun; Lee Chen-Chi; Hsieh Lie-Jiau; Chen Wen-Lin; Wang Wayseen
Molecular cytogenetic analysis of de novo dup(5)(q33.1q31.1) associated with abnormal perinatal findings.
Prenatal diagnosis 2006;26(2):181-3.
2006: Chen C P; Lin S P; Lee C C; Town D D; Wang W
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: Chen C P; Lin S P; Chern S R; Lee C C; Huang J K; Wang W
Direct transmission of the 18q- syndrome from mother to daughter.
Genetic counseling (Geneva, Switzerland) 2006;17(2):185-9.
2006: Chen Chih-Ping; Chang Tung-Yao; Su Yi-Ning; Hsu Chin-Yuan; Wang Wayseen
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: Chen C P; Lee C C; Town D D; Chen W L; Chen L F; Lee M S; Pan C W; Wang W
Detection of euchromatic variants and unusual C band heterochromatin variants at genetic amniocentesis.
Genetic counseling (Geneva, Switzerland) 2006;17(1):91-5.
2006: Chen C P; Lin S P; Lin C C; Li Y C; Hsieh L J; Huang J K; Lee C C; Wang W
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: Chen Chih-Ping; Lin Shuan-Pei; Lin Chyi-Chyang; Li Yueh-Chun; Hsieh Lie-Jiau; Chern Schu-Rern; Lee Chen-Chi; Chen Yen-Jiun; Wang Wayseen
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: Chen Chih-Ping; Chern Schu-Rern; Lin Shuan-Pei; Lin Chyi-Chyang; Li Yueh-Chun; Wang Tzu-Hao; Lee Chen-Chi; Pan Chen-Wen; Hsieh Lie-Jiau; Wang Wayseen
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: Chen Chih-Ping; Chern Schu-Rern; Chang Tung-Yao; Lee Chen-Chi; Chen Wen-Lin; Wang Wayseen
Prenatal diagnosis of partial trisomy 10q (10q25.3-->qter) and partial monosomy 18q (18q23-->qter).
Prenatal diagnosis 2005;25(11):1069-71.
2005: Chen Chih-Ping; Chern Schu-Rern; Chen Li-Feng; Chen Wen-Lin; Wang Wayseen
Prenatal diagnosis of low-level mosaic trisomy 7 by amniocentesis.
Prenatal diagnosis 2005;25(11):1067-9.
2005: Chen Chih-Ping; Hsu Chin-Yuan; Huang Jon-Kway; Lee Chen-Chi; Chen Wen-Lin; Wang Wayseen
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: Chen Chih-Ping; Lin Shuan-Pei; Lin Chyi-Chyang; Li Yueh-Chun; Hsieh Lie-Jiau; Lee Chen-Chi; Chen Yen-Jiun; Wang Wayseen
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: Chen Chih-Ping; Liu Yu-Peng; Lin Shuan-Pei; Sheu Jin-Cherng; Hsu Chin-Yuan; Chang Tung-Yao; Wang Wayseen
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: Chen Chih-Ping; Shih Jin-Chung; Hsu Chin-Yuan; Chen Chen-Yu; Huang Jon-Kway; Wang Wayseen
Prenatal three-dimensional/four-dimensional sonographic demonstration of facial dysmorphisms associated with holoprosencephaly.
Journal of clinical ultrasound : JCU 2005;33(6):312-8.
2005: Chen Chih-Ping; Shih Jin-Chung; Chang Tung-Yao; Chern Schu-Rern; Lin Ching-Yi; Wang Wayseen; Tzen Chin-Yuan
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: Chen Chih-Ping; Cheng Sho-Jen; Lin Yi-Hui; Wang Wayseen
Prenatal imaging of limb-body wall complex by magnetic resonance imaging.
Prenatal diagnosis 2005;25(6):521-3.
2005: Chen Chih-Ping; Chang Tung-Yao; Lin Shuan-Pei; Huang Jon-Kway; Tsai Jeng-Daw; Chiu Nan-Chang; Wang Wayseen
Prenatal magnetic resonance imaging of Galloway-Mowat syndrome.
Prenatal diagnosis 2005;25(6):525-7.
2005: Chen Chih-Ping; Liu Yu-Peng; Huang Jon-Kway; Chang Tung-Yao; Chen Ming-Ren; Chiu Nan-Chang; Wang Wayseen
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: Chen Chih-Ping; Chern Schu-Rern; Sheu Jin-Chern; Lin Shuan-Pei; Hsu Chin-Yuan; Chang Tung-Yao; Lee Chen-Chi; Wang Wayseen; Chen Hsiao-En Cindy
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: Chen Chih-Ping; Chern Schu-Rern; Wang Tzu-Hao; Hsueh Ding-Wei; Lee Chen-Chi; Town Dai-Dyi; Wang Wayseen; Ko Tsang-Ming
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: Chen Chih-Ping; Lin Shuan-Pei; Lee Chen-Chi; Chen Wen-Lin; Chen Li-Feng; Wang Wayseen
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: Chen Chih-Ping; Chern Schu-Rern; Chang Tung-Yao; Chen Wen-Lin; Chen Li-Feng; Wang Wayseen; Cindy Chen Hsiao-En
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: Chen Chih-Ping; Shih Jin-Chung; Tzen Chin-Yuan; Lin Yi-Hui; Wang Wayseen
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: Chen Chih-Ping; Chern Schu-Rern; Tsai Fuu-Jen; Lin Ching-Yi; Lin Yi-Hui; Wang Wayseen
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: Chen Chih-Ping; Chern Schu-Rern; Hsu Chin-Yuan; Lee Chen-Chi; Lee Meng-Shan; Wang Wayseen
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: Chen Chih-Ping; Chen Chen-Yu; Lin Ching-Yi; Shaw Sheng-Wen; Wang Wayseen; Tzen Chin-Yuan
Prenatal diagnosis of concomitant alobar holoprosencephaly and caudal regression syndrome associated with maternal diabetes.
Prenatal diagnosis 2005;25(3):264-6.
2005: Chen Chih-Ping; Chang Tung-Yao; Tzen Chin-Yuan; Wang Wayseen; Lee Chen-Chi
Recurrent fetal pyelectasis in a family with fetuses associated with partial trisomy 10q (10q24.1-->qter).
Prenatal diagnosis 2005;25(3):263-4.
2005: Chen Chih-Ping; Su Yi-Ning; Huang Jian-Pei; Lin Yi-Hui; Wang Wayseen
Asymmetrical terminal limb defects in a hydropic infant with homozygous alpha-thalassemia-1.
Prenatal diagnosis 2005;25(2):178-9.
2005: Chen Chih-Ping; Lin Shuan-Pei; Lin Chyi-Chyang; Li Yueh-Chun; Chern Schu-Rern; Chen Wei-Min; Lee Chen-Chi; Hsieh Lie-Jiau; Wang Wayseen
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: Chen Chih-Ping; Su Yi-Ning; Hung Chia-Cheng; Lee Chien-Nan; Hsieh Fon-Jou; Chang Tung-Yao; Chen Ming-Ren; Wang Wayseen
Molecular genetic analysis of the TSC genes in two families with prenatally diagnosed rhabdomyomas.
Prenatal diagnosis 2005;25(2):176-8.
2005: Chen C P; Chern S R; Lin C J; Lee C C; Wang W; Tzen C Y
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: Chen Chih-Ping; Sheu Jin-Chern; Huang Jon-Kway; Lin Yi-Hui; Tzen Chin-Yuan; Wang Wayseen
Second-trimester magnetic resonance imaging of fetal sacrococcygeal teratoma with intrapelvic extension in a co-twin.
Prenatal diagnosis 2004;24(12):1015-7.
2004: Chen Chih-Ping; Lee Chen-Chi; Wang Wayseen
Prenatal diagnosis of complete trisomy 16q in two consecutive pregnancies.
Prenatal diagnosis 2004;24(12):1019-20.
2004: Chen Chih-Ping; Lee Chen-Chi; Wang Wayseen
Prenatal diagnosis of complete trisomy 16q in two consecutive pregnancies.
Prenatal diagnosis 2004;24(11):928-9.
2004: Chen Chih-Ping; Hsu Chin-Yuan; Lee Chen-Chi; Chen Wen-Lin; Chen Li-Feng; Wang Wayseen
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: Chen Chih-Ping; Lin Chyi-Chyang; Li Yueh-Chun; Chern Schu-Rern; Lee Chen-Chi; Chen Wen-Lin; Lee Men-Shan; Wang Wayseen; Tzen Chin-Yuan
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: Chen Chih-Ping; Chern Schu-Rern; Lee Chen-Chi; Lin Shuan-Pei; Chang Tung-Yao; Wang Wayseen
Prenatal diagnosis of mosaic 22q11.2 microdeletion.
Prenatal diagnosis 2004;24(8):660-2.
2004: Chen Chih-Ping; Chern Schu-Rern; Cheng Sho-Jen; Chang Tung-Yao; Yeh Li-Fan; Lee Chen-Chi; Pan Chen-Wen; Wang Wayseen; Tzen Chin-Yuan
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: Chen Chih-Ping; Chern Schu-Rern; Lee Chen-Chi; Chen Wen-Lin; Wang Wayseen
Prenatal diagnosis of interstitially satellited 6p.
Prenatal diagnosis 2004;24(6):430-3.
2004: Chen Chih-Ping; Chang Tung-Yao; Lin Yi-Hui; Wang Wayseen
Prenatal sonographic diagnosis of acrania associated with amniotic bands.
Journal of clinical ultrasound : JCU 2004;32(5):256-60.
2004: Chen Chih-Ping; Hung Han-Yang; Chang Tung-Yao; Lin Shuan-Pei; Wang Wayseen
Second-trimester nasal bone hypoplasia/aplasia associated with cleidocranial dysplasia.
Prenatal diagnosis 2004;24(5):399-400.
2004: Chen Chih-Ping; Lin Shuan-Pei; Hwu Yuh-Ming; Chang Tung-Yao; Wang Wayseen
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: Chen Chih-Ping; Lin Shuan-Pei; Tzen Chin-Yuan; Tsai Fuu-Jen; Hwu Wuh-Liang; Wang Wayseen
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: Chen Chih-Ping; Chern Schu-Rern; Chang Tung-Yao; Tzen Chin-Yuan; Lee Chen-Chi; Chen Wen-Lin; Chen Li-Feng; Wang Wayseen
Prenatal diagnosis of the distal 11q deletion and review of the literature.
Prenatal diagnosis 2004;24(2):130-6.
2004: Chen C-P; Chang T-Y; Town D-D; Chen L-F; Pan C-W; Wang W; Tzen C-Y
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: Chen C-P; Cheng S-J; Chang T-Y; Yeh L-F; Lin Y-H; Wang W
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: Chen Chih-Ping; Shih Jin-Chung; Chern Schu-Rern; Lee Chen-Chi; Wang Wayseen
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: Chen Chih-Ping; Lee Chen-Chi; Chang Tung-Yao; Town Dai-Dyi; Wang Wayseen
Prenatal diagnosis of mosaic distal 5p deletion and review of the literature.
Prenatal diagnosis 2004;24(1):50-7.
2004: Chen Chih-Ping; Chern Schu-Rern; Lee Chen-Chi; Chang Tung-Yao; Wang Wayseen; Tzen Chin-Yuan
Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.
Prenatal diagnosis 2004;24(1):38-44.
2004: Chen Chih-Ping; Lee Chen-Chi; Chen Wen-Lin; Wang Wayseen; Tzen Chin-Yuan
Prenatal diagnosis of premature centromere division-related mosaic variegated aneuploidy.
Prenatal diagnosis 2004;24(1):19-25.
2004: Chen C P; Lee C C; Town D D; Lee M S; Wang W
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: Chen C P; Lin S P; Chern S R; Lee C C; Huang J K; Wang W; Liao Y W
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.
2003: Chen Chih-Ping; Chern Schu-Rern; Town Dai-Dyi; Wang Wayseen; Liao You-Wei
Fetoplacental and fetoamniotic chromosomal discrepancies in prenatally detected mosaic trisomy 9.
Prenatal diagnosis 2003;23(12):1019-21.
2003: Chen Chih-Ping; Chern Schu-Rern; Lee Chen-Chi; Chen Li-Feng; Chin Daniel T H; Tzen Chin-Yuan; Wang Wayseen
Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion.
Prenatal diagnosis 2003;23(9):758-61.
2003: Chen C-P; Shih J-C; Shih S-L; Huang J-K; Huang J-P; Lin Y-H; Wang W
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: Chen Chih-Ping; Shih Jin-Chung; Huang Jon-Kway; Wang Wayseen; Tzen Chin-Yuan
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: Chen Chih-Ping; Hsu Chyong-Hsin; Lin Shuan-Pei; Ho Che-Sheng; Lee Chen-Chi; Wang Wayseen
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: Chen Chih-Ping; Shih Jin-Chung; Chang Jui-Hsing; Lin Yi-Hui; Wang Wayseen
Prenatal diagnosis of right pulmonary agenesis associated with VACTERL sequence.
Prenatal diagnosis 2003;23(6):515-8.
2003: Chen Chih-Ping; Lin Shuan-Pei; Chern Schu-Rern; Shih Shin-Lin; Lee Chen-Chi; Wang Wayseen; Liao You-Wei
Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion.
Prenatal diagnosis 2003;23(6):504-8.
2003: Chen Chih-Ping; Chang Tung-Yao; Tzen Chin-Yuan; Wang Wayseen; Lee Chen-Chi; Chen Li-Feng; Lee Meng-Shan; Lin Shaun-Pei
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: Chen Chih-Ping; Chern Schu-Rern; Chang Tung-Yao; Tzen Chin-Yuan; Lee Chen-Chi; Chen Wen-Lin; Lee Meng-Shan; Wang Wayseen
Prenatal diagnosis of de novo terminal deletion of chromosome 7q.
Prenatal diagnosis 2003;23(5):375-9.
2003: Chen Chih-Ping; Hwu Yuh-Ming; Yeh Li-Fan; Chern Schu-Rern; Lee Chen-Chi; Wang Wayseen
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: Chen Chih-Ping; Chang Tung-Yao; Tzen Chin-Yuan; Wang Wayseen
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: Chen Chih-Ping; Chang Tung-Yao; Chern Schu-Rern; Town Dai-Dyi; Pan Chen-Wen; Lee Meng-Shan; Wang Wayseen
Early second-trimester diagnosis of monozygotic twins discordant for cystic hygroma colli and Turner syndrome.
Prenatal diagnosis 2003;23(4):352-3.
2003: Chen Chih-Ping; Chern Schu-Rern; Lin Shuan-Pei; Wang Wayseen; Tsai Fuu-Jen
Prenatal identification of a G338E mutation in FGFR2 in a fetus without sonographic appearance of craniosynostosis.
Prenatal diagnosis 2003;23(2):175-6.
2003: Chen Chih-Ping; Chern Schu-Rern; Chang Tung-Yao; Lee Chen-Chi; Chen Li-Feng; Tzen Chin-Yuan; Wang Wayseen; Lin Chen-Ju; Yang Brian P T; Yang Lawrence S T
Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction.
Prenatal diagnosis 2003;23(1):40-3.
2002: Chen Chih-Ping; Tzen Chin-Yuan; Chang Tung-Yao; Lin Chen-Ju; Wang Wayseen; Lee Chen-Chi; Town Dai-Dyi; Chen Li-Feng; Lee Meng-Shan
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: Chen Chih-Ping; Chang Tung-Yao; Shih Jin-Chung; Lin Shuan-Pei; Lin Chen-Ju; Wang Wayseen; Lee Chen-Chi; Town Dai-Dyi; Pan Chen-Wen; Tzen Chin-Yuan
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: Chen Chih-Ping; Lin Shuan-Pei; Chang Tung-Yao; Chiu Nan-Chang; Shih Shin-Lin; Lin Chen-Ju; Wang Wayseen; Hsu Hong-Chih
Perinatal imaging findings of inherited Sotos syndrome.
Prenatal diagnosis 2002;22(10):887-92.
2002: Chen Chih-Ping; Chern Schu-Rern; Chang Tung-Yao; Lin Chen-Ju; Wang Wayseen; Tzen Chin-Yuan
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: Chen C P; Tzen C Y; Chang T Y; Yeh L F; Wang W
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: Chen Chih-Ping; Yang Yuh-Cheng; Lin Shuan-Pei; Wang Wayseen; Chang Chih-Long; Chang Kuo-Ming
Bilateral calcified ovarian fibromas in a patient with Sotos syndrome.
Fertility and sterility 2002;77(6):1285-7.
2002: Chen Chih-Ping; Chang Tung-Yao; Yeh Li-Fan; Lin Chen-Ju; Wang Wayseen
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: Chen Chih-Ping; Sheu Jin-Cherng; Wang Wayseen; Lin Shuan-Pei; Chang Tung-Yao; Tzen Chin-Yuan
Fetal cervico-mediastinal cystic hygroma associated with maternal serum screening positive for Down syndrome.
Prenatal diagnosis 2002;22(2):166.
2002: Chen Chih-Ping; Chern Schu-Rern; Du Shin-Hua; Wang Wayseen
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: Chen C P; Chern S R; Wang W; Lee C C; Chen W L; Chen L F; Chang T Y; Tzen C Y
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: Chen C P; Chern S R; Wang W
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: Chen C P; Chern S R; Tzen C Y; Lee M S; Pan C W; Chang T Y; Wang W
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: Chen C P; Chern S R; Wang W; Wang K L; Wang T Y
Multiple globules in a cystic ovarian teratoma.
Fertility and sterility 2001;75(3):618-9.
2001: Chen C P; Chern S R; Lee C C; Chen W L; Wang W
Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly.
Prenatal diagnosis 2001;21(2):102-5.
2001: Chen C P; Chern S R; Shih J C; Wang W; Yeh L F; Chang T Y; Tzen C Y
Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasia.
Prenatal diagnosis 2001;21(2):89-95.
2000: Chen C P; Chern S R; Chang C L; Lee C C; Chen W L; Chen L F; Wang W
Prenatal diagnosis and genetic analysis of X chromosome polysomy 49, XXXXY.
Prenatal diagnosis 2000;20(9):754-7.
2000: Chen C P; Chern S R; Yeh L F; Chen W L; Chen L F; Wang W
Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18.
Prenatal diagnosis 2000;20(9):750-3.
2000: Chen C P; Devriendt K; Chern S R; Lee C C; Wang W; Lin S P
Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
Prenatal diagnosis 2000;20(5):384-9.
2000: Chen C P; Chern S R; Wang W
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: Chen C P; Devriendt K; Lee C C; Chen W L; Wang W; Wang T Y
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: Chen C P; Shih J C; Lee C C; Chen L F; Wang W; Wang T Y
Prenatal diagnosis of a fetus with distal 10q trisomy.
Prenatal diagnosis 1999;19(9):876-8.
1999: Chen C P; Chern S R; Lee C C; Town D D; Chen W L; Wang W
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: Chen C P; Chen S R; Wang T Y; Wang W; Hwu Y M
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: Chen C P; Chern S R; Wang T Y; Wang W; Wang K L; Jeng C J
Androgen receptor gene mutations in 46,XY females with germ cell tumours.
Human reproduction (Oxford, England) 1999;14(3):664-70.
1998: Chen C P; Wang W; Lin S P; Sheu J C; Tsai J D
Perinatal findings in a male fetus with congenital megacystis and anorectal malformations.
Fetal diagnosis and therapy 1998;13(6):348-51.

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