Showing 1 - 5 results of 5 for search 'Weiyue Gu', query time: 0.03s Refine Results
  1. 1
    Correction to: Digenic inheritance of SLC12A3 and CLCNKB genes in a Chinese girl with Gitelman syndrome

    Correction to: Digenic inheritance of SLC12A3 and CLCNKB genes in a Chinese girl with Gitelman syndrome by Yuanmei Kong, Ke Xu, Ke Yuan, Jianfang Zhu, Weiyue Gu, Li Liang, Chunlin Wang

    Published 2019
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  2. 2
    The first case of intellectual disability caused by novel compound heterozygosity for NUDT2 variants

    The first case of intellectual disability caused by novel compound heterozygosity for NUDT2 variants by Bo Bi, Xiaohong Chen, Shan Huang, Min Peng, Weiyue Gu, Hongmin Zhu, Yangcan Ming

    Published 2024
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  3. 3
    Case Report: Novel CA12 Homozygous Variant Causing Isolated Hyperchloridrosis in a Chinese Child With Hyponatremia

    Case Report: Novel CA12 Homozygous Variant Causing Isolated Hyperchloridrosis in a Chinese Child With Hyponatremia by Meigui Han, Min Peng, Ziming Han, Xiaojuan Zhu, Qian Huang, Weiyue Gu, Yong Guo

    Published 2022
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  4. 4
    Digenetic inheritance of SLC12A3 and CLCNKB genes in a Chinese girl with Gitelman syndrome

    Digenetic inheritance of SLC12A3 and CLCNKB genes in a Chinese girl with Gitelman syndrome by Yuanmei Kong, Ke Xu, Ke Yuan, Jianfang Zhu, Weiyue Gu, Li Liang, Chunlin Wang

    Published 2019
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  5. 5
    A comprehensive multiplex PCR based exome-sequencing assay for rapid bloodspot confirmation of inborn errors of metabolism

    A comprehensive multiplex PCR based exome-sequencing assay for rapid bloodspot confirmation of inborn errors of metabolism by Wenjie Wang, Jianping Yang, Jinjie Xue, Wenjuan Mu, Xiaogang Zhang, Wang Wu, Mengnan Xu, Yuyan Gong, Yiqian Liu, Yu Zhang, Xiaobing Xie, Weiyue Gu, Jigeng Bai, David S. Cram

    Published 2019
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