English  |  正體中文  |  简体中文  |  Items with full text/Total items : 90069/105176 (86%)
Visitors : 6470967      Online Users : 537
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
    HomeLoginUploadHelpAboutAdminister Goto mobile version

    Category

    Loading community tree, please wait....

    Year

    Loading year class tree, please wait....

    Items for Author "Huang, Jian-Pei" 

    Return to Browse by Author

    Showing 5 items.

    Collection Date Title Authors Bitstream
    [生物科技學系] 期刊論文 Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review 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
    [生物科技學系] 期刊論文 Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review 陳持平; Chen, Chih-Ping; Hua, Jian-Pei; Huang, Jian-Pei; Chen, Yi-Yung; Chen, Yi-Yung; 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, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes 陳持平; Chen, Chih-Ping; Hua, Jian-Pei; Huang, Jian-Pei; Chen, Yi-Yung; Chen, Yi-Yung; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Pan, Chen-Wen; Pan, Chen-Wen; Wang, Wayseen; Wang, Wayseen
    [生物科技學系] 期刊論文 2013-10 Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review 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
    [生物科技學系] 期刊論文 2010-06 Fetal magnetic resonance imaging demonstration of central nervous system abnormalities and polydactyly associated with Joubert syndrome 陳持平; Chen, Chih-Ping; Su, Yi-Ning; Huang, Jon-Kway; Liu, Yu-Peng; Tsai, Fuu-Jen; Yang, Chun-Kuang; Huang, Jian-Pei; Chen, Chen-Yu; Wu, Pei-Chen; Wang, Wayseen

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