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

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  2. Dr Thomas Berney
  3. Daniela Pinto
  4. Professor Ann Le Couteur
  5. 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
JournalJournal of Medical Genetics
Year2011
Volume48
Issue1
Pages48-54
ISSN (print)0022-2593
ISSN (electronic)1468-6244
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PublisherBMJ Group
URLhttp://dx.doi.org/10.1136/jmg.2010.079426
DOI10.1136/jmg.2010.079426
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