Hasil Pencarian - Ti-Long Huang

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  1. 1
    Clinical and whole-exome sequencing findings in two siblings from Hani ethnic minority with congenital glycosylation disorders

    Clinical and whole-exome sequencing findings in two siblings from Hani ethnic minority with congenital glycosylation disorders oleh Zhen Zhang, Ti-Long Huang, Jing Ma, Wen-Ji He, Huaiyu Gu

    Diterbitkan 2019-11-01
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  2. 2
    A de novo ANK1 mutation associated to hereditary spherocytosis: a case report

    A de novo ANK1 mutation associated to hereditary spherocytosis: a case report oleh Ti-Long Huang, Bao-Hua Sang, Qing-Ling Lei, Chun-Yan Song, Yun-Bi Lin, Yu Lv, Chun-Hui Yang, Na Li, Yue-Huang Yang, Xian-Wen Zhang, Xin Tian

    Diterbitkan 2019-02-01
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  3. 3
    Gene Mutation Spectrum of Thalassemia Among Children in Yunnan Province

    Gene Mutation Spectrum of Thalassemia Among Children in Yunnan Province oleh Ti-Long Huang, Tian-Yao Zhang, Chun-Yan Song, Yun-Bi Lin, Bao-Hua Sang, Qing-Ling Lei, Yu Lv, Chun-Hui Yang, Na Li, Xin Tian, Yue-Huang Yang, Xian-Wen Zhang

    Diterbitkan 2020-04-01
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