Showing 1 - 4 results of 4 for search 'Mei-Guang Zhang', query time: 0.03s Refine Results
  1. 1
    Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population

    Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population by Xue Gao, Sha-Sha Huang, Yong-Yi Yuan, Jin-Cao Xu, Ping Gu, Dan Bai, Dong-Yang Kang, Ming-Yu Han, Guo-Jian Wang, Mei-Guang Zhang, Jia Li, Pu Dai

    Published 2017-01-01
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  2. 2
    Novel compound heterozygous mutations in MYO7A Associated with Usher syndrome 1 in a Chinese family.

    Novel compound heterozygous mutations in MYO7A Associated with Usher syndrome 1 in a Chinese family. by Xue Gao, Guo-Jian Wang, Yong-Yi Yuan, Feng Xin, Ming-Yu Han, Jing-Qiao Lu, Hui Zhao, Fei Yu, Jin-Cao Xu, Mei-Guang Zhang, Jiang Dong, Xi Lin, Pu Dai

    Published 2014-01-01
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    Article
  3. 3
    Correction: Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family.

    Correction: Novel Compound Heterozygous Mutations in MYO7A Associated with Usher Syndrome 1 in a Chinese Family. by Xue Gao, Guo-Jian Wang, Yong-Yi Yuan, Feng Xin, Ming-Yu Han, Jing-Qiao Lu, Hui Zhao, Fei Yu, Jin-Cao Xu, Mei-Guang Zhang, Jiang Dong, Xi Lin, Pu Dai

    Published 2015-01-01
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    Article
  4. 4
    Identification of Two Novel Compound Heterozygous PTPRQ Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family.

    Identification of Two Novel Compound Heterozygous PTPRQ Mutations Associated with Autosomal Recessive Hearing Loss in a Chinese Family. by Xue Gao, Yu Su, Yu-Lan Chen, Ming-Yu Han, Yong-Yi Yuan, Jin-Cao Xu, Feng Xin, Mei-Guang Zhang, Sha-Sha Huang, Guo-Jian Wang, Dong-Yang Kang, Li-Ping Guan, Jian-Guo Zhang, Pu Dai

    Published 2015-01-01
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    Article

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