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A novel single-base deletion in ROR2 causes atypical brachydactyly type B1 with cutaneous syndactyly
  • ISSN号：1434-5161
  • 期刊名称：Journal of Human Genetics
  • 时间：0
  • 页码：422-425
  • 语言：英文
  • 相关项目：重要出生缺陷遗传致病基因的识别及功能研究
作者： Sun, Miao|Lo, Wilson H-Y|Wen, Yaran|Zhao, Xiuli|Yang, Wei|Cao, Lihua|Luo, Yang|Lv, Dan|Zhang, Xue|
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重要出生缺陷遗传致病基因的识别及功能研究
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