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Article

A novel de-novo WNT5A mutation in a Chinese patient with Robinow syndrome.

Clinical dysmorphology - 1 Oct 2016

Xiong Shiyi, Chitayat David, Wei Xing, Zhu Jialiang, Lu Wen, Sun Lu Ming, Chopra Maya

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PMID: 27092434
DOI: 10.1097/MCD.0000000000000130

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Related research

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A novel de-novo WNT5A mutation in a Chinese patient with Robinow syndrome.PMID 27092434Read ↗

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Biallelic loss-of-function WNT5A mutations in an infant with severe and atypical manifestations of Robinow syndrome.Semantic proximity Read ↗

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