作者
- Chen, C.P. (12)
- Chen, L.F. (6)
- Chen, S.W. (4)
- Chen, Y.N. (12)
- Chern, S.R. (9)
- Kuo, Y.L. (3)
- Pan, C.W. (3)
- Wang, W. (12)
- Wu, P.S. (10)
- Yang, C.W. (6)
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總筆數:12
| 篇名 | 作者 | 刊名 | 出版年 | 查看 |
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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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| First-trimester diagnosis of recurrent omphalocele associated withfetal trisomy 18 but without parental mosaicism |
Chen, C.P.;Wang, L.K.;Chern, S.R.;Kuo, Y.L.;Chen, Y.N.;Pan, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2015-04-01 |
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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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| Pregnancy with de novo 9q34.3 microdeletion and Kleefstra syndrome inthe fetus may be associated with an abnormal maternal serum screening result |
Chen, C.P.;Lin, S.P.;Li, H.B.;Chen, Y.N.;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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