Human Genome Epidemiology Literature Finder

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Query Trace: Intellectual Disability and ASTN2[original query]
Clinical significance of de novo and inherited copy-number variation. Human mutation 2013 Dec 34 (12): 1679-87. Vulto-van Silfhout Anneke T, Hehir-Kwa Jayne Y, van Bon Bregje W M, Schuurs-Hoeijmakers Janneke H M, Meader Stephen, Hellebrekers Claudia J M, Thoonen Ilse J M, de Brouwer Arjan P M, Brunner Han G, Webber Caleb, Pfundt Rolph, de Leeuw Nicole, de Vries Bert B Similar articles in PubMed