| 篇名 | 作者 | 刊名 | 出版年 | 查看 |
|---|
| Array-CGH detection of UGT2B28 gene deletion in a girl with primaryamenorrhea and hyperandrogenism |
Zhang, Y.;Dai, Y.;Tu, Z.;Li, Q.;Wang, L.;Zhang, L.; |
International Journal of Gynecology & Obstetrics |
2010-05-01 |
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| Array-CGH detection of UGT2B28 gene deletion in a girl with primaryamenorrhea and hyperandrogenism |
Zhang, Y.;Dai, Y.;Tu, Z.;Li, Q.;Wang, L.;Zhang, L.; |
International Journal of Gynecology & Obstetrics |
2010-05-01 |
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| Mosaic Ring Chromosome 18, Ring Chromosome 18 Duplication/Deletion andDisomy 18: Perinatal Findings and Molecular Cytogenetic Characterization byFluorescence In Situ Hybridization and Array Comparative GenomicHybridization |
Chen, C.P.;Kuo, Y.T.;Lin, S.P.;Su, Y.N.;Chen, Y.J.;Hsueh, R.Y.;Lin, Y.H.;Wu, P.C.;Lee, C.C.;Chen, Y.T.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-09-01 |
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| Inv dup del(9p): Prenatal diagnosis and molecular cytogeneticcharacterization by fluorescence in situ hybridization and arraycomparative genomic hybridization |
Chen, C.P.;Su, Y.N.;Chern, S.R.;Hsu, C.Y.;Tsai, F.J.;Wu, P.C.;Lee, C.C.;Chen, Y.T.;Lee, M.S.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-03-01 |
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| Prenatal diagnosis and molecular cytogenetic characterization ofmosaicism for a small supernumerary marker chromosome derived from ringchromosome 4 |
Chen, C.P.;Chen, M.;Su, Y.N.;Tsai, F.J.;Chern, S.R.;Wu, P.C.;Chen, W.L.;Chen, L.F.;Pan, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-06-01 |
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| Molecular strategies for pre-implantation genetic diagnosis of singlegene and chromosomal disorders |
Jiang, B.;Tan, A.S.C.;Chong, S.S.; |
Best Practice & Research in Clinical Obstetrics and Gynaecology |
2012-10-01 |
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| Rapid positive confirmation of mosaicism for a small supernumerarymarker chromosome as r(8) by interphase fluorescence in situ hybridization,quantitative fluorescent polymerase chain reaction, and array comparativegenomic hybridization on uncultured amniocytes in a pregnancy with fetalpyelectasis |
Chen, C.P.;Chang, S.D.;Su, Y.N.;Chen, M.;Chern, S.R.;Su, J.W.;Chen, Y.T.;Chen, W.L.;Pan, C.W.;Lee, M.S.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2012-09-01 |
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| Partial trisomy 8 mosaicism not detected by cultured amniotic-fluidcells |
Tsai, M.C.;Cheng, H.Y.;Su, M.T.;Chen, M.;Kuo, P.L.; |
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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| 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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| Detection of recurrent 4p16.3 microdeletion with 2p25.3microduplication by multiplex ligation-dependent probe amplification andarray comparative genomic hybridization in a fetus from a family withWolf-Hirschhorn syndrome |
Yang, W.X.;Pan, H.;Wang, S.T.;Li, L.;Wu, H.R.;Qi, Y.; |
Taiwanese Journal of Obstetrics and Gynecology |
2016-02-01 |
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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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