2019 Clinical dysmorphology
DOI PubMed

Changing facial features in a child with GAPO syndrome caused by novel mutation in the ANTXR1 gene and uniparental disomy of chromosome 2.

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Clinical dysmorphology Vol. 28 (4) : 211-214 • Oct 2019

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Paper Details
PMID: 31425299
DOI: 10.1097/MCD.0000000000000292 [doi]
Publication Year: 2019
Language: e, n, g
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