Showing 1 - 2 results of 2 for search 'Yuanyuan lian', query time: 0.02s Refine Results
  1. 1
    A Novel Compound Heterozygous Variant in the ABHD12 Gene Cause PHARC Syndrome in a Chinese Family: The Proband Presenting New Genotype and Phenotype

    A Novel Compound Heterozygous Variant in the ABHD12 Gene Cause PHARC Syndrome in a Chinese Family: The Proband Presenting New Genotype and Phenotype by Meijiao Ma, Jinhai Ma, Yuanyuan Lian, Xueli Wu, Wenming Wang, Weining Rong, Xunlun Sheng

    Published 2025-02-01
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  2. 2
    Whole-exome sequencing screening for candidate genes and potential pathogenic variants associated with early-onset high myopia in 47 Chinese families

    Whole-exome sequencing screening for candidate genes and potential pathogenic variants associated with early-onset high myopia in 47 Chinese families by Xue Rui, Huiping Li, Runqing Ma, Shangying Yang, Yuanyuan lian, Wanyu Cheng, Meijiao Ma, Weining Rong, Xunlun Sheng

    Published 2025-04-01
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