English  |  正體中文  |  简体中文  |  Items with full text/Total items : 90453/105672 (86%)
Visitors : 13172852      Online Users : 618
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 "Shih-Ting La" 

    Return to Browse by Author

    Showing 10 items.

    Collection Date Title Authors Bitstream
    [生物科技學系] 期刊論文 2017-08 Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect 陳持平; Chih-Ping Chen; Chen-Yu Chen; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Chen-Chi Lee; Chien-Wen Ya; Chien-Wen Yang; Wayseen Wang
    [生物科技學系] 期刊論文 2017-08 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16 陳持平; Chih-Ping Chen; Tsang-Ming K; Tsang-Ming Ko; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Chien-Wen Ya; Chien-Wen Yang; Chen-Wen Pan; Wayseen Wang
    [生物科技學系] 期刊論文 2017-08 Prenatal diagnosis of mosaicism for trisomy 2 in a single colony at amniocentesis in a pregnancy with a favorable outcome 陳持平; Chih-Ping Chen; Jian-Pei Hua; Jian-Pei Huang; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Chen-Chi Lee; Chien-Wen Ya; Chien-Wen Yang; Wayseen Wang
    [生物科技學系] 期刊論文 2017-08 Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9 陳持平; Chih-Ping Chen; Ming Chen; Liang-Kai Wa; Liang-Kai Wang; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Shun-Ping Ch; Shun-Ping Chang; Chien-Wen Ya; Chien-Wen Yang; Chen-Wen Pan; Wayseen Wang
    [生物科技學系] 期刊論文 2017-06 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11 陳持平; Chih-Ping Chen; Ming Chen; Pu-Tsui Wang; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Shun-Ping Ch; Shun-Ping Chang; Chen-Wen Pan; Wayseen Wang
    [生物科技學系] 期刊論文 2017-06 Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q ；2q31.1-q32.1 encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency 陳持平; Chih-Ping Chen; Chen-Ju Lin; Yen-Ni Chen; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Li-Feng Chen; Wayseen Wang
    [生物科技學系] 期刊論文 2017-06 Molecular genetic characterization of a prenatally detected 1.484-Mb Xq13.3-q21.1 duplication encompassing ATRX and a literature review of syndromic intellectual disability and congenital abnormalities in males with a duplication at Xq13.3-q21.1 陳持平; Chih-Ping Chen; Hoi-Kin Yip; Liang-Kai Wa; Liang-Kai Wang; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Wayseen Wang
    [生物科技學系] 期刊論文 2017-06 Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 20p ；20p12-p13 encompassing JAG1 and a literature review of prenatal diagnosis of Alagille syndrome 陳持平; Chih-Ping Chen; Chang-Sheng; Chang-Sheng Yin; Liang-Kai Wa; Liang-Kai Wang; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Wen-Lin Chen; Wayseen Wang
    [生物科技學系] 期刊論文 2017-06 Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 7 in the male partner of a phenotypically normal couple with repeated spontaneous abortions 陳持平; Chih-Ping Chen; Ming Chen; Yuh-Ming Hwu; Shun-Ping Ch; Shun-Ping Chang; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Chen-Chi Lee; Wayseen Wang
    [生物科技學系] 期刊論文 2017-06 Pfeiffer syndrome with FGFR2 C342R mutation presenting extreme proptosis, craniosynostosis, hearing loss, ventriculomegaly, broad great toes and thumbs, maxillary hypoplasia, and laryngomalacia 陳持平; Chih-Ping Chen; Shuan-Pei Li; Shuan-Pei Lin; Yu-Peng Liu; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Wayseen Wang

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