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Diagnostic and clinical utility of whole genome sequencing in a cohort of undiagnosed Chinese families with rare diseases

Diagnostic and clinical utility of whole genome sequencing in a cohort of undiagnosed Chinese families with rare diseases

Liu, Hong-Yan; Zhou, Liyuan; Zheng, Meng-Yue; Huang, Jia; Wan, Shu; Zhu, Aiying; Zhang, Mingjie; Dong, Anliang; Hou, Ling; Li, Jia; Xu, Haiming; Lu, Bingjian; Lu, Weiguo; Liu, Pengyuan; Lu, Yan
  • 期刊名称Scientific Reports
  • 作者Liu, Hong-Yan; Zhou, Liyuan; Zheng, Meng-Yue; Huang, Jia; Wan, Shu; Zhu, Aiying; Zhang, Mingjie; Dong, Anliang; Hou, Ling; Li, Jia; Xu, Haiming; Lu, Bingjian; Lu, Weiguo; Liu, Pengyuan; Lu, Yan
  • 卷第9卷
  • 期第1期
  • 电子ISSN2045-2322
  • 文件大小3189.92KB
  • 发表时间2019-12
  • DOI10.1038/s41598-019-55832-1
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