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

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Description scientific article
Author/s

author: Massimo Molteni  James S. Sutcliffe  Stephen W. Scherer  Maria Clara Bonaglia  Roberto Giorda  Kirsty Wing  Ann Le Couteur  Tom Berney  Peter Szatmari  Veronica J Vieland  Dianne Gerrelli  Joachim Hallmayer  Andrew D. Paterson  Anthony Monaco  Dalila Pinto  Alistair T Pagnamenta 

Publication date January 2011
Language English
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