Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability
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author: Roberto Giorda, Kirsty Wing, Dalila Pinto, Massimo Molteni, James S. Sutcliffe, Maria Clara Bonaglia, Andrew D. Paterson, Anthony Monaco, Peter Szatmari, Stephen W. Scherer, Veronica J Vieland, Alistair T Pagnamenta, Tom Berney, Ann Le Couteur, Joachim Hallmayer, Dianne Gerrelli
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