English  |  正體中文  |  简体中文  |  Items with full text/Total items : 90069/105176 (86%)
Visitors : 6448787      Online Users : 578
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
    •  Adv. Search
    Home ‧ Login ‧ Upload ‧ Help ‧ About ‧ Administer Goto mobile version

    Category

    Loading community tree, please wait....

    Year

    Loading year class tree, please wait....

    Items for Author "陳持平*" 

    Return to Browse by Author

    Showing 11 items.

    Collection Date Title Authors Bitstream
    [生物科技學系] 期刊論文 2016-02 Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion Chen), Yen-Ni Chen(Yen-Ni; 陳持平*; Ko), Tsang-Ming K(Tsang-Ming; Wang), Liang-Kai Wa(Liang-Kai; Wu), Pei-Chen Wu(Pei-Chen; Chang), Tung-Yao Cha(Tung-Yao; Wu), Peih-Shan Wu(Peih-Shan; Yang), Chien-Wen Ya(Chien-Wen; Wang), Wayseen Wang(Wayseen
    [生物科技學系] 期刊論文 2016-02 Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion Chen, Yen-Ni; Chen, Yen-Ni; 陳持平*; Tsang-Ming, K; Ko, Tsang-Ming; Wa, Liang-Kai; Wang, Liang-Kai; Wu, Pei-Chen; Wu, Pei-Chen; Cha, Tung-Yao; Chang, Tung-Yao; Wu, Peih-Shan; Wu, Peih-Shan; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2015-10 Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome and Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1 陳持平*; Lin), Ming-Huei Li(Ming-Huei; Chen), Yi-Yung Chen(Yi-Yung; Chern), Schu-Rern Ch(Schu-Rern; Chen), Yen-Ni Chen(Yen-Ni; Wu), Peih-Shan Wu(Peih-Shan; Pan), Chen-Wen Pan(Chen-Wen; Lee), Meng-Shan Le(Meng-Shan; Wang), Wayseen Wang(Wayseen
    [生物科技學系] 期刊論文 2015-08 Pregnancy with de novo 9q34.3 microdeletion and Kleefstra syndrome in the fetus may be associated with an abnormal maternal serum screening result 陳持平*; Lin), Shuan-Pei Li(Shuan-Pei; Li), Hui-Bo Li(Hui-Bo; Chen), Yen-Ni Chen(Yen-Ni; Wang), Wayseen Wang(Wayseen
    [生物科技學系] 期刊論文 2015-08 Mosaic trisomy 15 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review 陳持平*; Chern), Schu-Rern Ch(Schu-Rern; Chen), Yen-Ni Chen(Yen-Ni; Wu), Peih-Shan Wu(Peih-Shan; Yang), Chien-Wen Ya(Chien-Wen; Chen), Li-Feng Chen(Li-Feng; Wang), Wayseen Wang(Wayseen
    [生物科技學系] 期刊論文 2015-06 Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature 陳持平*; Huang), Ming-Chao Hu(Ming-Chao; Chern), Schu-Rern Ch(Schu-Rern; Kuo), Yu-Ling Kuo(Yu-Ling; Chen), Yen-Ni Chen(Yen-Ni; Wu), Peih-Shan Wu(Peih-Shan; Chen), Li-Feng Chen(Li-Feng; Pan), Chen-Wen Pan(Chen-Wen; Wang), Wayseen Wang(Wayseen
    [生物科技學系] 期刊論文 2015-04 First-trimester diagnosis of recurrent omphalocele associated with fetal trisomy 18 but without parental mosaicism 陳持平*; Wa, Liang-Kai; Wang, Liang-Kai; Ch, Schu-Rern; Chern, Schu-Rern; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Yen-Ni; Chen, Yen-Ni; Pan, Chen-Wen; Pan, Chen-Wen; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2015-02 Detection of no isochromosome 20q by interphase fluorescence in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis 陳持平*; Su, Jun-Wei; Su, Jun-Wei; Ch, Schu-Rern; Chern, Schu-Rern; Kuo, Yu-Ling; Kuo, Yu-Ling; Wu, Peih-Shan; Wu, Peih-Shan; Le, Meng-Shan; Lee, Meng-Shan; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2015-02 Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma 陳持平*; Tsang-Ming, K; Ko, Tsang-Ming; Hu, Ming-Chao; Huang, Ming-Chao; Ch, Schu-Rern; Chern, Schu-Rern; Lin, Tan-Wei; Lin, Tan-Wei; Cha, Tung-Yao; Chang, Tung-Yao; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2015-02 Detection of no isochromosome 20q by interphase fluorescent in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis 陳持平*; Su, Jun-Wei; Su, Jun-Wei; Ch, Schu-Rern; Chern, Schu-Rern; Kuo, Yu-Ling; Kuo, Yu-Ling; Wu, Peih-Shan; Wu, Peih-Shan; Le, Meng-Shan; Lee, Meng-Shan; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2015-02 Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diap 陳持平*; Wan, Yeou-Lih; Wang, Yeou-Lih; Ch, Schu-Rern; Chern, Schu-Rern; Liu, Yu-Peng; Liu, Yu-Peng; Pe, Cheng-Ran; Peng, Cheng-Ran; Kuo, Yu-Ling; Kuo, Yu-Ling; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback