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IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features

✍ Scribed by Erin L. Youngs; Rebecca Henkhaus; Jessica A. Hellings; Merlin G. Butler

Book ID: 116433424
Publisher: Elsevier Science
Year: 2012
Tongue: English
Weight: 498 KB
Volume: 55
Category: Article
ISSN: 1769-7212
DOI: 10.1016/j.ejmg.2011.08.004

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