Showing 1 - 3 results of 3 for search 'Wang Qing K', query time: 0.02s Refine Results
  1. 1
    Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosa

    Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosa by Huang Yukan, Zhang Jing, Li Chang, Yang Guohua, Liu Mugen, Wang Qing K, Tang Zhaohui

    Published 2010
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  2. 2
    A novel <it>DSPP </it>mutation is associated with type II dentinogenesis Imperfecta in a chinese family

    A novel <it>DSPP </it>mutation is associated with type II dentinogenesis Imperfecta in a chinese family by Xu Chengqi, Wang Xiaotao, Chang Wei, Zhao Zhen, Qu Erjun, Chen Lanying, Liu Jingyu, Zhang Xianqin, Wang Qing K, Liu Mugen

    Published 2007
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  3. 3
    Protective effect of <it>KCNH2 </it>single nucleotide polymorphism K897T in LQTS families and identification of novel <it>KCNQ1 </it>and <it>KCNH2 </it>mutations

    Protective effect of <it>KCNH2 </it>single nucleotide polymorphism K897T in LQTS families and identification of novel <it>KCNQ1 </it>and <it>KCNH2 </it>mutations by Oberti Carlos, Redfearn Sharon, Bryant Randall M, Liu Mugen, Zhang Li, Chen Shenghan, Zhang Xianqin, Vincent G Michael, Wang Qing K

    Published 2008
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