Hasil Pencarian - Hongqin GAO

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  1. 1
    Characterization of four common deafness gene mutations among 12 221 newborns delivered at four hospitals in a district of Suzhou city, 2018 – 2022

    Characterization of four common deafness gene mutations among 12 221 newborns delivered at four hospitals in a district of Suzhou city, 2018 – 2022 oleh Yuxing FAN, Hongqin GAO, Hong PAN, Yong XU, Hong ZHU

    Diterbitkan 2024-02-01
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  2. 2
    Insights into the assembly of the neovaginal microbiota in Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome patients

    Insights into the assembly of the neovaginal microbiota in Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome patients oleh Na Chen, Lilan Hao, Zhe Zhang, Chenglu Qin, Zhuye Jie, Hongxin Pan, Jiali Duan, Xincheng Huang, Yunhong Zhang, Hongqin Gao, Ruike Lu, Tianshu Sun, Hua Yang, Jinqiu Shi, Maolian Liang, Jianbin Guo, Qianqian Gao, Xiaoyue Zhao, Zhiyuan Dou, Liang Xiao, Shaoqiao Zhang, Xin Jin, Xun Xu, Huanming Yang, Jian Wang, Huijue Jia, Tao Zhang, Karsten Kristiansen, Chen Chen, Lan Zhu

    Diterbitkan 2024-09-01
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