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總筆數:27

篇名作者刊名出版年查看
Primary Unruptured Ovarian Pregnancy at 12 Weeks of Gestation Chang, T.Y.;Wang, K.G.;Chen, C.Y.;Chen, C.P.;Tzen, C.Y.;Yu, S.L.;Kuo, S.C.; Taiwanese Journal of Obstetrics and Gynecology 2004-09-01 查看
Effects of Antenatal Betamethasone and Dexamethasone in Preterm Neonates Chen, C.Y.;Wang, K.G.;Chang, T.Y.;Chen, C.P.;Loo, J.H.; Taiwanese Journal of Obstetrics and Gynecology 2005-09-01 查看
Third-trimester Ultrasound Evaluation of Arachnoid Cysts Chen, C.P.;Chang, T.Y.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2007-12-01 查看
Third-trimester Ultrasound Evaluation of Arachnoid Cysts Chen, C.P.;Chang, T.Y.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2007-12-01 查看
Prenatal Magnetic Resonance Imaging, Ultrasound Imaging Findings andGenetic Analysis of Concomitant Rhabdomyomas and Cerebral Tuberous Sclerosis Chen, C.P.;Su, Y.N.;Chang, T.Y.;Liu, Y.P.;Tsai, F.J.;Hwang, J.K.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2009-09-01 查看
Prenatal Diagnosis of Monosomy 17p (17p 13.3 @? pter) Associated WithPolyhydramnios, Intrauterine Growth Restriction, Ventriculomegaly, andMiller-Dieker Lissencephaly Syndrome in a Fetus Lin, C.Y.;Chen, C.P.;Liau, C.L.;Su, P.H.;Tsao, T.F.;Chang, T.Y.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2009-12-01 查看
22q 11.2 Microdeletion in a Fetus With Double-outlet Right Ventricle,Pulmonary Stenosis and a Ventricular Septal Defect: Prenatal Diagnosis byArray Comparative Genomic Hybridization Chen, C.P.;Su, Y.N.;Chang, T.Y.;Chern, S.R.;Tsai, F.J.;Hwang, J.K.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2009-12-01 查看
Prenatal Diagnosis of Monosomy 17p (17p 13.3 -> pter) Associated WithPolyhydramnios, Intrauterine Growth Restriction, Ventriculomegaly, andMiller-Dieker Lissencephaly Syndrome in a Fetus Lin, C.Y.;Chen, C.P.;Liau, C.L.;Su, P.H.;Tsao, T.F.;Chang, T.Y.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2009-12-01 查看
22q 11.2 Microdeletion in a Fetus With Double-outlet Right Ventricle,Pulmonary Stenosis and a Ventricular Septal Defect: Prenatal Diagnosis byArray Comparative Genomic Hybridization Chen, C.P.;Su, Y.N.;Chang, T.Y.;Chern, S.R.;Tsai, F.J.;Hwang, J.K.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2009-12-01 查看
Prenatal Diagnosis of Persistent Cloaca With Hydrometrocolpos andAscites by Magnetic Resonance Imaging in One Fetus of a Dizygotic TwinPregnancy Chen, C.P.;Liu, Y.P.;Chang, T.Y.;Tsai, F.J.;Chen, C.Y.;Wu, P.C.;Chen, T.H.T.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2010-09-01 查看
Prenatal Diagnosis of Rhabdomyomas and Cerebral Tuberous Sclerosis byMagnetic Resonance Imaging in One Fetus of a Dizygotic Twin PregnancyAssociated With a Frameshift Mutation in the TSC2 Gene Chen, C.P.;Su, Y.N.;Chang, T.Y.;Liu, Y.P.;Tsai, F.J.;Chen, M.R.;Hwang, J.K.;Chen, T.H.T.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2010-09-01 查看
Short rib-polydactyly syndrome type II (Majewski): Prenatal diagnosis,perinatal imaging findings and molecular analysis of the NEK1 gene Chen, C.P.;Chang, T.Y.;Chen, C.Y.;Wang, T.Y.;Tsai, F.J.;Wu, P.C.;Chern, S.R.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2012-03-01 查看
Prenatal diagnosis and molecular genetic analysis of shortrib-polydactyly syndrome type III (Verma-Naumoff) in a second-trimesterfetus with a homozygous splice site mutation in intron 4 in the NEK1 gene Chen, C.P.;Chern, S.R.;Chang, T.Y.;Su, Y.N.;Chen, Y.Y.;Su, J.W.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2012-06-01 查看
Osteogenesis imperfecta type I: Second-trimester diagnosis andincidental identification of a dominant COL1A1 deletion mutation in thepaucisymptomatic father Chen, C.P.;Su, Y.N.;Chang, T.Y.;Chern, S.R.;Chen, C.Y.;Su, J.W.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2012-06-01 查看
Identification of a deletion mutation in the short flanking repeatregion of exon 44 of the COL1A1 gene in a fetus with osteogenesisimperfecta type II Chen, C.P.;Su, Y.N.;Chang, T.Y.;Chern, S.R.;Su, J.W.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2012-06-01 查看
Osteogenesis imperfecta type II: Prenatal diagnosis and associationwith increased nuchal translucency and hypoechogenicity of the cranium Chen, C.P.;Su, Y.N.;Chang, T.Y.;Huang, M.C.;Pan, C.H.;Chern, S.R.;Su, J.W.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2012-06-01 查看
Rapid detection of de novo P253R mutation in FGFR2 using unculturedamniocytes in a pregnancy affected by polyhydramnios, Blake's pouch cyst,and Apert syndrome Chen, C.P.;Su, Y.N.;Chang, T.Y.;Chern, S.R.;Chen, C.Y.;Su, J.W.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2013-06-01 查看
Detection of maternal transmission of a splicing mutation in the TSC2gene following prenatal diagnosis of fetal cardiac rhabdomyomas mimickingcongenital cystic adenomatoid malformation of the lung and cerebral tubersand awareness of a family history of maternal epilepsy Chen, C.P.;Chang, T.Y.;Guo, W.Y.;Su, Y.N.;Chen, Y.Y.;Chern, S.R.;Su, J.W.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2013-09-01 查看
Rapid detection of K650E mutation in FGFR3 using uncultured amniocytesin a pregnancy affected with fetal cloverleaf skull, occipitalpseudoencephalocele, ventriculomegaly, straight short femurs, andthanatophoric dysplasia type II Chen, C.P.;Chang, T.Y.;Lin, M.H.;Chern, S.R.;Su, J.W.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2013-09-01 查看
Detection of maternal transmission of a splicing mutation in the TSC2gene following prenatal diagnosis of fetal cardiac rhabdomyomas mimickingcongenital cystic adenomatoid malformation of the lung and cerebral tubersand awareness of a family history of maternal epilepsy Chen, C.P.;Chang, T.Y.;Guo, W.Y.;Su, Y.N.;Chen, Y.Y.;Chern, S.R.;Su, J.W.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2013-09-01 查看
Rapid detection of K650E mutation in FGFR3 using uncultured amniocytesin a pregnancy affected with fetal cloverleaf skull, occipitalpseudoencephalocele, ventriculomegaly, straight short femurs, andthanatophoric dysplasia type II Chen, C.P.;Chang, T.Y.;Lin, M.H.;Chern, S.R.;Su, J.W.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2013-09-01 查看
VACTERL association with hydrocephalus in a fetus conceived by in vitrofertilization and embryo transfer Chen, C.P.;Chang, T.Y.;Chen, Y.Y.;Chern, S.R.;Su, J.W.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2013-12-01 查看
Detection of a de novo Y278C mutation in FGFR3 in a pregnancy withsevere fetal hypochondroplasia: Prenatal diagnosis and literature review Chen, C.P.;Su, Y.N.;Lin, T.H.;Chang, T.Y.;Su, J.W.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2013-12-01 查看
Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemannsyndrome in a pregnancy conceived by intracytoplasmic sperm injection andin vitro fertilization and embryo transfer Chen, C.P.;Su, Y.N.;Chen, S.U.;Chang, T.Y.;Wu, P.C.;Chern, S.R.;Wu, P.S.;Kuo, Y.L.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2014-03-01 查看
Detection of de novo secondary trisomy 13 due to isochromosome(13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma Chen, C.P.;Ko, T.M.;Huang, M.C.;Chern, S.R.;Lin, T.W.;Chang, T.Y.;Kuo, Y.L.;Chen, W.L.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2015-02-01 查看
Prenatal diagnosis of chromosome 8p23.1 microdeletion by arraycomparative genomic hybridization using uncultured amniocytes in apregnancy associated with fetal partial corpus callosum agenesis andschizencephaly Chen, C.P.;Peng, C.R.;Chang, T.Y.;Guo, W.Y.;Chen, Y.N.;Wu, P.S.;Town, D.D.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2015-12-01 查看
Prenatal diagnosis of 22q11.2 deletion syndrome associated with rightaortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion Chen, Y.N.;Chen, C.P.;Ko, T.M.;Wang, L.K.;Wu, P.C.;Chang, T.Y.;Wu, P.S.;Yang, C.W.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2016-02-01 查看
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