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    Items for Author "Liang-Kai Wa" 

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    Showing 4 items.

    Collection Date Title Authors Bitstream
    [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 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 2017-04 Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome 陳持平; Chih-Ping Chen; Tsang-Ming K; Tsang-Ming Ko; Liang-Kai Wa; Liang-Kai Wang; Shuan-Pei Li; Shuan-Pei Lin; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Che; Shin-Wen Chen; Meng-Shan Le; Meng-Shan Lee; Wayseen Wang

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