Disruption of PCP signaling causes limb morphogenesis and skeletal defects and may underlie Robinow syndrome and brachydactyly type B
出版年份 2010 全文链接
标题
Disruption of PCP signaling causes limb morphogenesis and skeletal defects and may underlie Robinow syndrome and brachydactyly type B
作者
关键词
-
出版物
HUMAN MOLECULAR GENETICS
Volume 20, Issue 2, Pages 271-285
出版商
Oxford University Press (OUP)
发表日期
2010-10-21
DOI
10.1093/hmg/ddq462
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