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"su jun wei"的相关文件
显示项目 11-20 / 31 (共4页)
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| 亞洲大學 |
201309 |
De novo unbalanced translocation resulting in monosomy for distal 5p (5p14.1->pter) and 14q (14q32.31->qter) associated with fetal nuchal edema, microcephaly, intrauterine growth restriction and single umbilical artery: prenatal diagnosis and molecular
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陳持平;Chen, Chih-Ping;Fu, Chung-Hu;Fu, Chung-Hu;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Lee, Chen-Chi;Lee, Chen-Chi;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Detection of maternal transmission of a splicing mutation in the TSC2 gene following prenatal diagnosis of fetal cardiac rhabdomyomas mimicking congenital cystic adenomatoid malformation of the lung and cerebral tubers and awareness of a family history of
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陳持平;Chen, Chih-Ping;Cha, Tung-Yao;Chang, Tung-Yao;Guo, Wan-Yuo;Guo, Wan-Yuo;Su, Yi-Ning;Su, Yi-Ning;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straight short femurs and thanatophoric dysplasia type II
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陳持平;Chen, Chih-Ping;Cha, Tung-Yao;Chang, Tung-Yao;Li, Ming-Huei;Lin, Ming-Huei;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Mosaic trisomy 14 at amniocentesis: prenatal diagnosis and literature review
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陳持平;Chen, Chih-Ping;Wang, Kuo-Gon;Wang, Kuo-Gon;Tsang-Ming, K;Ko, Tsang-Ming;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Town, Dai-Dyi;Town, Dai-Dyi;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Application of interphase fluorescence in situ hybridization to uncultured amniocytes for differential diagnosis of pseudomosaicism from true mosaicism in mosaic isochromosome 20q detected at amniocentesis
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陳持平;Chen, Chih-Ping;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Chen, Li-Feng;Chen, Li-Feng;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Prenatal diagnosis of mosaic trisomy 12 associated with congenital overgrowth
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陳持平;Chen, Chih-Ping;Ch, Shing-Jyh;Chang, Shing-Jyh;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-10 |
An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsy
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陳持平;Chen, Chih-Ping;Li, Shuan-Pei;Lin, Shuan-Pei;Liu, Yu-Peng;Liu, Yu-Peng;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Lee, Chen-Chi;Lee, Chen-Chi;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-10 |
Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review
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陳持平;Chen, Chih-Ping;Chen, Ming;Chen, Ming;Su, Yi-Ning;Su, Yi-Ning;Hua, Jian-Pei;Huang, Jian-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Ch, Shun-Ping;Chang, Shun-Ping;Chen, Li-Feng;Chen, Li-Feng;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-09 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome
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陳持平;Chen, Chih-Ping;Tsang-Ming, K;Ko, Tsang-Ming;Chen, Yi-Yung;Su, Jun-Wei;Wang, Wayseen; |
| 亞洲大學 |
2013-07 |
6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia, psychomotor developmental delay and poor wound healing
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陳持平;Chen, Chih-Ping;Li, Shuan-Pei;Lin, Shuan-Pei;Liu, Yu-Peng;Liu, Yu-Peng;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yu-Ting;Chen, Yu-Ting;Su, Jun-Wei;Su, Jun-Wei;Lee, Chen-Chi;Lee, Chen-Chi;Wang, Wayseen;Wang, Wayseen |
显示项目 11-20 / 31 (共4页)
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