De Novo Mutations inFOXP1in Cases with Intellectual Disability, Autism, and Language Impairment


Fadi F. Hamdan,Hussein Daoud,Daniel Rochefort,Amélie Piton,Julie Gauthier,Mathieu Langlois,Gila Foomani,Sylvia Dobrzeniecka,Marie-Odile Krebs,Ridha Joober,Ronald G. Lafrenière,Jean-Claude Lacaille,Laurent Mottron,Pierre Drapeau,Miriam H. Beauchamp, et al.


The American Journal of Human Genetics




12 November 2010

Copyright © 2010, Elsevier

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