Search Results - Gaoxiong Wang

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    A case report: Marfan syndrome with X trisomy and FBN1 and SDHB mutations by Jiansheng Lin, Yanyu Lin, Gaoxiong Wang

    Published 2023
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    A de novo PAK1 likely pathogenic variant and a de novo terminal 1q microdeletion in a Chinese girl with global developmental delay, severe intellectual disability, and seizures by Jianlong Zhuang, Meihua Xie, Jianfeng Yao, Wanyu Fu, Shuhong Zeng, Yuying Jiang, Yuanbai Wang, Yingjun Xie, Gaoxiong Wang, Chunnuan Chen

    Published 2023
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