Showing 1 - 2 results of 2 for search 'Wei-Qian Wang', query time: 0.02s Refine Results
  1. 1
    A novel variant in FOXC1 associated with atypical Axenfeld-Rieger syndrome

    A novel variant in FOXC1 associated with atypical Axenfeld-Rieger syndrome by Rui Wang, Wei-Qian Wang, Xiao-Qin Li, Juan Zhao, Kun Yang, Yong Feng, Meng-Meng Guo, Min Liu, Xing Liu, Xi Wang, Yong-Yi Yuan, Xue Gao, Jin-Cao Xu

    Published 2021
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  2. 2
    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
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