Search Results - Liangliang Fan

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    Case report: A de novo Non-sense SOX9 mutation (p.Q417*) located in transactivation domain is Responsible for Campomelic Dysplasia by Xingxing Qiao, Liping Wu, Liping Wu, Jianjun Tang, Rong Xiang, Rong Xiang, Rong Xiang, Liangliang Fan, Liangliang Fan, Liangliang Fan, Hao Huang, Hao Huang, Hao Huang, Yaqin Chen

    Published 2023
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    Case Report: A Novel Heterozygous Mutation of CD2AP in a Chinese Family With Proteinuria Leads to Focal Segmental Glomerulosclerosis by Yu-Xing Liu, Yu-Xing Liu, Yu-Xing Liu, Yu-Xing Liu, Ai-Qian Zhang, Fang-Mei Luo, Fang-Mei Luo, Yue Sheng, Yue Sheng, Chen-Yu Wang, Chen-Yu Wang, Yi Dong, Yi Dong, Liangliang Fan, Liangliang Fan, Liangliang Fan, Liangliang Fan, Lv Liu

    Published 2021
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