Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

Dr Thomas Berney; Daniela Pinto; Professor Ann Le Couteur; Dr Andrew Paterson

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability Lookup NU author(s) Dr Thomas Berney Daniela Pinto Professor Ann Le Couteur Dr Andrew Paterson



Author(s)		Pagnamenta AT, Khan H, Walker S, Gerrelli D, Wing K, Bonaglia MC, Giorda R, Berney T, Mani E, Molteni M, Pinto D, Le Couteur A, Hallmayer J, Sutcliffe JS, Szatmari P, Paterson AD, Scherer SW, Vieland VJ, Monaco AP
Publication type		Article
Journal		Journal of Medical Genetics
Year		2011
Volume		48
Issue		1
Pages		48-54
ISSN (print)		0022-2593
ISSN (electronic)		1468-6244



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Publisher		BMJ Group
URL		http://dx.doi.org/10.1136/jmg.2010.079426
DOI		10.1136/jmg.2010.079426

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