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Schu-Rern Chern

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Second Pregnancy Trimester

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Co-Publications
Name
72
Wang, Wayseen
61
Chen, Chih-Ping
36
Lee, Chen-Chi
24
Chang, Tung-Yao
22
Tzen, Chin-Yuan
19
Lin, Shuan-Pei
13
Tsai, Fuu-Jen
13
Chen, Wen-Lin
10
Town, Dai-Dyi
9
Chen, Li-Feng
9
Lin, Chyi-Chyang
8
Hsieh, Lie-Jiau
7
Lee, Meng-Shan
7
Wang, Tzu-Hao
6
Li, Yueh-Chun

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Publications

TOP 3
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.
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.

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All Publications

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; 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: Tzeng Ruu-Fen; Liu Shen-Ing; Wu Lawrence S H; Chen Shu-Ting; Yu Yen-Hsin; Li Pei-Chuan; Chern Schu-Rern; Lee Pei-Yin; Lan Tsuo-Hung; Loh El-Wui
High proportion of single CYP2D6 gene deletion in Chinese attention-deficit-hyperactivity disorder children and its risk in oppositional defiant disorder.
Psychiatry and clinical neurosciences 2008;62(6):749.
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; 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.
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 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; 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; 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: Liu Chien-Liang; Chang Yuan-Ching; Cheng Shih-Ping; Chern Schu-Rern; Yang Tsen-Long; Lee Jie-Jen; Guo Ing-Cherng; Chen Chih-Ping
The roles of serum leptin concentration and polymorphism in leptin receptor gene at codon 109 in breast cancer.
Oncology 2007;72(1-2):75-81.
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 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; 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; 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; 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 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; 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; 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.
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; 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; 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; 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; 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; 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 Hui-Ju; Lin Shuan-Pei; Lee Hung-Chang; Chen Chih-Ping; Chiu Nan-Chang; Hung Han-Yang; Chern Schu-Rern; Chuang Chih-Kuang
Cystic fibrosis with homozygous R553X mutation in a Taiwanese child.
Journal of human genetics 2005;50(12):674-8.
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; 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; 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 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; 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 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 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; 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; 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; 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 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; 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; Chern S R; Chen B F; Wang W; Hwu Y M
Hamartoma in a pubertal patient with complete androgen insensitivity syndrome and R(831)X mutation of the androgen receptor gene.
Fertility and sterility 2000;74(1):182-3.
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: Chern S R; Chen C P
Molecular prenatal diagnosis of thalassemia in Taiwan.
International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics 2000;69(2):103-6.
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; 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; 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; Chern S R; Lee C C; Chen W L; Chen M H; Chang K M
De novo unbalanced translocation resulting in monosomy for proximal 14q and distal 4p in a fetus with intrauterine growth retardation, Wolf-Hirschhorn syndrome, hypertrophic cardiomyopathy, and partial hemihypoplasia.
Journal of medical genetics 1998;35(12):1050-3.
1998: Chen C P; Chern S R; Lee C C; Town D D
Isochromosome 18q in a fetus with congenital megacystis, intra-uterine growth retardation and cloacal dysgenesis sequence.
Prenatal diagnosis 1998;18(10):1068-74.
1998: Chen C P; Chern S R; Lin S P; Chang P Y; Chang K M; Hsieh F J
Concomitant chyloperitoneum and omental cysts presenting as fetal ascites with intra-abdominal cysts on prenatal ultrasound.
Prenatal diagnosis 1998;18(9):984-6.
1998: Chen C P; Chern S R; Lee C C; Chen L F; Chuang C Y
Prenatal diagnosis of de novo interstitial 16q deletion in a fetus associated with sonographic findings of prominent coronal sutures, a prominent frontal bone, and shortening of the long bones.
Prenatal diagnosis 1998;18(5):490-5.
1998: Chen C P; Chern S R; Lee C C; Chen L F; Chuang C Y; Chen M H
Prenatal diagnosis of de novo isochromosome 13q associated with microcephaly, alobar holoprosencephaly and cebocephaly in a fetus.
Prenatal diagnosis 1998;18(4):393-8.
1998: Chen C P; Chern S R; Chuang C Y; Chen B F
Prenatal detection of human cytomegalovirus DNA in fetal ascites by the polymerase chain reaction.
Acta obstetricia et gynecologica Scandinavica 1998;77(4):466-7.
1998: Chen C P; Chern S R; Shih S L; Chuang C Y; Huang F Y
Kyphomelic dysplasia in two sib fetuses.
Journal of medical genetics 1998;35(1):65-9.
1997: Chen C P; Chern S R; Wang T Y; Huang Z D; Huang M C; Chuang C Y
Pregnancy with concomitant chorangioma and placental vascular malformation with mesenchymal hyperplasia.
Human reproduction (Oxford, England) 1997;12(11):2553-6.
1997: Chen C P; Chern S R; Liu F F; Jan S W; Lee C C; Chang Y C; Yue C T
Prenatal diagnosis of a deletion of 18q in a fetus associated with multiple-marker screen positive results.
Prenatal diagnosis 1997;17(6):571-6.
1997: Chen C P; Chen H C; Liu F F; Jan S W; Chern S R; Wang T Y; Hung H Y
Cutis marmorata telangiectatica congenita associated with an elevated maternal serum human chorionic gonadotrophin level and transitory isolated fetal ascites.
The British journal of dermatology 1997;136(2):267-71.
1997: Chen C P; Chern S R; Liu F F; Jan S W; Lee H C; Sheu J C; Lee W T; Wang T Y
Prenatal diagnosis, pathology, and genetic study of fetus in fetu.
Prenatal diagnosis 1997;17(1):13-21.

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