Showing 1 - 2 results of 2 for search 'Liyuan Shang', query time: 0.03s Refine Results
  1. 1
    A novel compound heterozygous variation in the FKBP10 gene causes Bruck syndrome without congenital contractures: A case report

    A novel compound heterozygous variation in the FKBP10 gene causes Bruck syndrome without congenital contractures: A case report by Liyuan Shang, Weizhe Shi, Yibo Xu, Tianying Nong, Xia Li, Zhaohui Li, Yanhan Liu, Jingchun Li, Ya-Ping Tang, Mingwei Zhu, Hongwen Xu

    Published 2024-04-01
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    Article
  2. 2
    Novel de novo TRPV4 mutation identified in a Chinese family with metatropic dysplasia inhibits chondrogenic differentiation

    Novel de novo TRPV4 mutation identified in a Chinese family with metatropic dysplasia inhibits chondrogenic differentiation by Ping Wei, Weizhe Shi, Tianying Nong, Caixia Xian, Xia Li, Zhaohui Li, Xin Li, Jianping Wu, Liyuan Shang, Fulong Xu, Yibo Xu, Hongwen Xu, Mingwei Zhu

    Published 2024-05-01
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    Article

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