Disruption of PCP signaling causes limb morphogenesis and skeletal defects and may underlie Robinow syndrome and brachydactyly type B

Author: Wang Bing   Sinha Tanvi   Jiao Kai   Serra Rosa   Wang Jianbo  

Publisher: Oxford University Press

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.20, Iss.2, 2011-01, pp. : 271-285

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