☆ 3.9 Letter

Sporadic NF1 mutation associated with a de-novo 20q11.3 deletion explains the association of unusual facies, Moyamoya vasculopathy, and developmental delay, reported by Bertoli et al. in 2009

CLINICAL DYSMORPHOLOGY (2013)

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Journal

CLINICAL DYSMORPHOLOGY
Volume 22, Issue 1, Pages 42-43

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MCD.0b013e32835b8ea4

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Genetics & Heredity

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