Showing 1 - 3 results of 3 for search 'Xiru Wu', query time: 0.03s Refine Results
  1. 1
    Novel MEF2C point mutations in Chinese patients with Rett (−like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation

    Novel MEF2C point mutations in Chinese patients with Rett (−like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation by Jiaping Wang, Qingping Zhang, Yan Chen, Shujie Yu, Xiru Wu, Xinhua Bao, Yongxin Wen

    Published 2018
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  2. 2
    Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation

    Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation by Qingping Zhang, Jiaping Wang, Jiarui Li, Xinhua Bao, Ying Zhao, Xiaoying Zhang, Liping Wei, Xiru Wu

    Published 2017
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  3. 3
    SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures

    SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures by Jiaping Wang, Hua Gao, Xinhua Bao, Qingping Zhang, Jiarui Li, Liping Wei, Xiru Wu, Yan Chen, Shujie Yu

    Published 2017
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