作者
- Chen, C.P. (34)
- Chen, L.F. (11)
- Chen, Y.N. (10)
- Chen, Y.T. (11)
- Chern, S.R. (32)
- Kuo, Y.L. (11)
- Lee, M.S. (8)
- Su, J.W. (16)
- Wang, W. (34)
- Wu, P.S. (34)
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總筆數:34
篇名 | 作者 | 刊名 | 出版年 | 查看 |
Prenatal diagnosis and molecular cytogenetic characterization ofmosaicism for a small supernumerary marker chromosome derived from ringchromosome 2 |
Chen, C.P.;Chen, M.;Chern, S.R.;Wu, P.S.;Chang, S.P.;Lee, D.J.;Chen, Y.T.;Chen, L.F.;Su, J.W.;Hwa-Ruey Hsieh, A.;Hwa-Jiun Hsieh, A.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2012-09-01 |
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Mosaic trisomy 2 at amniocentesis: Prenatal diagnosis and moleculargenetic analysis |
Chen, C.P.;Su, Y.N.;Chern, S.R.;Chen, Y.T.;Wu, P.S.;Su, J.W.;Pan, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2012-12-01 |
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Prenatal diagnosis of an interstitial deletion of 10q (10q11.21 ->q21.1): Array comparative genomic hybridization characterization andliterature review |
Chen, C.P.;Su, Y.N.;Chern, S.R.;Wu, P.S.;Su, J.W.;Town, D.D.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2012-12-01 |
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Application of interphase FISH to uncultured amniocytes for rapidconfirmation of true trisomy 2 mosaicism in the case of suspected amniocytemosaicism involving trisomy 2 in a single colony |
Chen, C.P.;Hung, F.Y.;Chern, S.R.;Wu, P.S.;Su, J.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2013-06-01 |
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Maternal transmission of interstitial microdeletion in 5q13.2 detectedduring prenatal diagnosis of coarctation of the aorta |
Chen, C.P.;Lin, C.J.;Chen, C.Y.;Chern, S.R.;Wu, P.S.;Su, J.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2013-06-01 |
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Prenatal diagnosis of a distal 3p deletion associated withfetoplacental chromosomal discrepancy and confined placental mosaicismdetected by array comparative genomic hybridization |
Chen, C.P.;Chen, Y.Y.;Chern, S.R.;Wu, P.S.;Su, J.W.;Chen, W.L.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2013-06-01 |
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Discordant anencephaly and Cantrell syndrome in monozygotic twinsconceived by ICSI and IVF-ET |
Chen, C.P.;Huang, M.C.;Chern, S.R.;Wu, P.S.;Su, J.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2013-06-01 |
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Application of interphase fluorescence in situ hybridization touncultured amniocytes for differential diagnosis of pseudomosaicism fromtrue mosaicism in mosaic isochromosome 20q detected at amniocentesis |
Chen, C.P.;Chern, S.R.;Wu, P.S.;Su, J.W.;Chen, Y.T.;Chen, L.F.;Pan, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2013-09-01 |
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Prenatal diagnosis of mosaic trisomy 2 associated with abnormalmaternal serum screening, oligohydramnios, intrauterine growth restriction,ventricular septal defect, preaxial polydactyly, and facial dysmorphism |
Chen, C.P.;Chen, Y.Y.;Chern, S.R.;Wu, P.S.;Su, J.W.;Chen, Y.T.;Lee, C.C.;Chen, L.F.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2013-09-01 |
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De novo unbalanced translocation resulting in monosomy for distal 5p(5p14.1 -> pter) and 14q (14q32.31 -> qter) associated with fetal nuchaledema, microcephaly, intrauterine growth restriction, and single umbilicalartery: Prenatal diagnosis and molecular cytogenetic characterization |
Chen, C.P.;Fu, C.H.;Chern, S.R.;Wu, P.S.;Su, J.W.;Lee, C.C.;Lee, M.S.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2013-09-01 |
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Prenatal diagnosis of mosaic trisomy 2 associated with abnormalmaternal serum screening, oligohydramnios, intrauterine growth restriction,ventricular septal defect, preaxial polydactyly, and facial dysmorphism |
Chen, C.P.;Chen, Y.Y.;Chern, S.R.;Wu, P.S.;Su, J.W.;Chen, Y.T.;Lee, C.C.;Chen, L.F.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2013-09-01 |
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De novo unbalanced translocation resulting in monosomy for distal 5p(5p14.1 -> pter) and 14q (14q32.31 -> qter) associated with fetal nuchaledema, microcephaly, intrauterine growth restriction, and single umbilicalartery: Prenatal diagnosis and molecular cytogenetic characterization |
Chen, C.P.;Fu, C.H.;Chern, S.R.;Wu, P.S.;Su, J.W.;Lee, C.C.;Lee, M.S.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2013-09-01 |
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Application of interphase fluorescence in situ hybridization touncultured amniocytes for differential diagnosis of pseudomosaicism fromtrue mosaicism in mosaic isochromosome 20q detected at amniocentesis |
Chen, C.P.;Chern, S.R.;Wu, P.S.;Su, J.W.;Chen, Y.T.;Chen, L.F.;Pan, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2013-09-01 |
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Detection of recurrent transmission of 17q12 microdeletion by arraycomparative genomic hybridization in a fetus with prenatally diagnosedhydronephrosis, hydroureter, and multicystic kidney, and variable clinicalspectrum in the family |
Chen, C.P.;Chang, S.D.;Wang, T.H.;Wang, L.K.;Tsai, J.D.;Liu, Y.P.;Chern, S.R.;Wu, P.S.;Su, J.W.;Chen, Y.T.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2013-12-01 |
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A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2duplication detected by array comparative genomic hybridization in anadolescent girl with autism and difficulty in self-care of menstruation |
Chen, C.P.;Lin, S.P.;Chern, S.R.;Wu, P.S.;Su, J.W.;Lee, C.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2014-03-01 |
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Mosaic tetrasomy 9p at amniocentesis: Prenatal diagnosis, molecularcytogenetic characterization, and literature review |
Chen, C.P.;Wang, L.K.;Chern, S.R.;Wu, P.S.;Chen, Y.T.;Kuo, Y.L.;Chen, W.L.;Lee, M.S.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2014-03-01 |
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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 |
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Interphase FISH on uncultured amniocytes at repeat amniocentesis forrapid diagnosis of true mosaicism in a case of level II mosaicism involvingtrisomy 21 in a single colony from an in situ culture of amniocytes |
Chen, C.P.;Wang, P.T.;Lin, S.P.;Chern, S.R.;Chen, Y.T.;Wu, P.S.;Kuo, Y.L.;Chen, W.L.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2014-03-01 |
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Directly transmitted 4.5-Mb triplication of 4q12-q13.1: Prenataldiagnosis and molecular cytogenetic characterization |
Chen, C.P.;Lin, M.H.;Chern, S.R.;Chen, Y.T.;Wu, P.S.;Kuo, Y.L.;Lee, M.S.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2014-03-01 |
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Interphase FISH on uncultured amniocytes at repeat amniocentesis forrapid confirmation of low-level mosaicism for tetrasomy 18p |
Chen, C.P.;Lin, C.L.;Ko, T.M.;Chern, S.R.;Chen, Y.T.;Wu, P.S.;Kuo, Y.L.;Lee, M.S.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2014-03-01 |
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Prenatal diagnosis and molecular cytogenetic characterization ofmosaicism for a small supernumerary marker chromosome derived fromchromosome 15 |
Chen, C.P.;Chen, M.;Su, Y.N.;Chern, S.R.;Wu, P.S.;Chang, S.P.;Kuo, Y.L.;Chen, W.L.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2014-03-01 |
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Interphase fluorescence in situ hybridization characterization ofmosaicism using uncultured amniocytes and cultured stimulated cord bloodlymphocytes in prenatally detected Pallister-Killian syndrome |
Chen, C.P.;Peng, C.R.;Chern, S.R.;Kuo, Y.L.;Wu, P.S.;Town, D.D.;Pan, C.W.;Yang, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2014-12-01 |
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Prenatal diagnosis and molecular cytogenetic characterization of a1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1haploinsufficiency and Sotos syndrome |
Chen, C.P.;Lin, C.J.;Chern, S.R.;Liu, Y.P.;Kuo, Y.L.;Chen, Y.N.;Wu, P.S.;Town, D.D.;Chen, L.F.;Yang, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2014-12-01 |
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Detection of no isochromosome 20q by interphase fluorescent in situhybridization on uncultured amniocytes in a pregnancy with mosaicisochromosome 20q in cultured amniocytes at amniocentesis |
Chen, C.P.;Su, J.W.;Chern, S.R.;Kuo, Y.L.;Wu, P.S.;Lee, M.S.;Yang, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2015-02-01 |
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Prenatal diagnosis and array comparative genomic hybridizationcharacterization of trisomy 21 in a fetus associated with right congenitaldiaphragmatic hernia and a review of the literature of chromosomalabnormalities associated with congenital diaphragmatic hernia |
Chen, C.P.;Wang, Y.L.;Chern, S.R.;Liu, Y.P.;Peng, C.R.;Kuo, Y.L.;Wu, P.S.;Chen, W.L.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2015-02-01 |
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Distal 3p duplication and terminal 7q deletion associated with nuchaledema and cyclopia in a fetus and a review of the literature |
Chen, C.P.;Huang, M.C.;Chern, S.R.;Kuo, Y.L.;Chen, Y.N.;Wu, P.S.;Chen, L.F.;Pan, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2015-06-01 |
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Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, moleculargenetic analysis and literature review |
Chen, C.P.;Chern, S.R.;Chen, Y.N.;Wu, P.S.;Yang, C.W.;Chen, L.F.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2015-08-01 |
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Prenatal diagnosis and array comparative genomic hybridizationcharacterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13associated with Langer-Giedion syndrome, Cornelia de Lange syndrome andhaploinsufficiency of TRPS1, RAD21 and EXT1 |
Chen, C.P.;Lin, M.H.;Chen, Y.Y.;Chern, S.R.;Chen, Y.N.;Wu, P.S.;Pan, C.W.;Lee, M.S.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2015-10-01 |
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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 |
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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 |
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Prenatal diagnosis and molecular cytogenetic characterization of a denovo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2haploinsufficiency and tetralogy of Fallot |
Chen, C.P.;Chen, C.Y.;Chern, S.R.;Wu, P.S.;Chen, Y.N.;Chen, S.W.;Chen, L.F.;Yang, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2016-04-01 |
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Prenatal diagnosis and molecular cytogenetic characterization oflow-level true mosaicism for trisomy 21 using uncultured amniocytes |
Chen, C.P.;Wang, Y.L.;Chern, S.R.;Wu, P.S.;Chen, Y.N.;Chen, S.W.;Chen, L.F.;Lee, M.S.;Yang, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2016-04-01 |
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Prenatal diagnosis and molecular cytogenetic characterization of denovo partial monosomy 3p (3p26.3->pter) and partial trisomy 16q(16q23.1->qter) |
Chen, C.P.;Hung, F.Y.;Chern, S.R.;Wu, P.S.;Chen, Y.N.;Chen, S.W.;Lee, C.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2016-04-01 |
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Prenatal diagnosis of low-level mosaicism for trisomy 2 associated witha favorable pregnancy outcome |
Chen, C.P.;Ko, T.M.;Chern, S.R.;Wu, P.S.;Chen, Y.N.;Chen, S.W.;Chen, L.F.;Yang, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2016-04-01 |
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