Showing 1 - 6 results of 6 for search 'Pu Dai', query time: 0.06s Refine Results
  1. 1
    Clinical and molecular findings in a Chinese family with a de novo mitochondrial A1555G mutation

    Clinical and molecular findings in a Chinese family with a de novo mitochondrial A1555G mutation by Ping Gu, Guojian Wang, Xue Gao, Dongyang Kang, Pu Dai, Shasha Huang

    Published 2022
    Connect to this object online.
    Book
    Save to List
    Saved in:
  2. 2
    Identification of Novel TMC1 Compound Heterozygous Mutations Related to Autosomal Recessive Hearing Loss by Targeted Capture Sequencing

    Identification of Novel TMC1 Compound Heterozygous Mutations Related to Autosomal Recessive Hearing Loss by Targeted Capture Sequencing by Xue Gao, Sha-Sha Huang, Yu Su, Jin-Cao Xu, Pu Dai

    Published 2016
    Connect to this object online.
    Book
    Save to List
    Saved in:
  3. 3
    Variant analysis of 92 Chinese Han families with hearing loss

    Variant analysis of 92 Chinese Han families with hearing loss by Xiaohua Jin, Shasha Huang, Lisha An, Chuan Zhang, Pu Dai, Huafang Gao, Xu Ma

    Published 2022
    Connect to this object online.
    Book
    Save to List
    Saved in:
  4. 4
    Analysis of the genotype-phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients

    Analysis of the genotype-phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients by Ying Fu, Shasha Huang, Xue Gao, Mingyu Han, Guojian Wang, Dongyang Kang, Yongyi Yuan, Pu Dai

    Published 2022
    Connect to this object online.
    Book
    Save to List
    Saved in:
  5. 5
    Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families

    Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families by Yu Su, Xue Gao, Sha-Sha Huang, Jing-Ning Mao, Bang-Qing Huang, Jian-Dong Zhao, Dong-Yang Kang, Xin Zhang, Pu Dai

    Published 2018
    Connect to this object online.
    Book
    Save to List
    Saved in:
  6. 6
    Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site variants in MYO15A

    Addition of an affected family member to a previously ascertained autosomal recessive nonsyndromic hearing loss pedigree and systematic phenotype-genotype analysis of splice-site v... by Jin-Yuan Yang, Wei-Qian Wang, Ming-Yu Han, Sha-Sha Huang, Guo-Jian Wang, Yu Su, Jin-Cao Xu, Ying Fu, Dong-Yang Kang, Kun Yang, Xin Zhang, Xing Liu, Xue Gao, Yong-Yi Yuan, Pu Dai

    Published 2022
    Connect to this object online.
    Book
    Save to List
    Saved in:

Search Tools: