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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

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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

Print publication date: 23/10/2010

ISSN (print): 0022-2593

ISSN (electronic): 1468-6244

Publisher: BMJ Group

URL: http://dx.doi.org/10.1136/jmg.2010.079426

DOI: 10.1136/jmg.2010.079426


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