Works by Hao, Xiaoyan


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    Genetic and Clinical Features of Heterotaxy in a Prenatal Cohort.

    Published in:
    Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.818241
    By:
    • Yi, Tong;
    • Sun, Hairui;
    • Fu, Yuwei;
    • Hao, Xiaoyan;
    • Sun, Lin;
    • Zhang, Ye;
    • Han, Jiancheng;
    • Gu, Xiaoyan;
    • Liu, Xiaowei;
    • Guo, Yong;
    • Wang, Xin;
    • Zhou, Xiaoxue;
    • Zhang, Siyao;
    • Yang, Qi;
    • Fan, Jiaqi;
    • He, Yihua
    Publication type:
    Article
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    Rare KCND3 Loss-of-Function Mutation Associated With the SCA19/22.

    Published in:
    Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.919199
    By:
    • Li, Mengjie;
    • Liu, Fen;
    • Hao, Xiaoyan;
    • Fan, Yu;
    • Li, Jiadi;
    • Hu, Zhengwei;
    • Shi, Jingjing;
    • Fan, Liyuan;
    • Zhang, Shuo;
    • Ma, Dongrui;
    • Guo, Mengnan;
    • Xu, Yuming;
    • Shi, Changhe
    Publication type:
    Article
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