De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment-Reference-Cited by-同舟云学术

De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment

Published:2010-11 Issue:5 Volume:87 Page:671-678
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Hamdan Fadi F.,Daoud Hussein,Rochefort Daniel,Piton Amélie,Gauthier Julie,Langlois Mathieu,Foomani Gila,Dobrzeniecka Sylvia,Krebs Marie-Odile,Joober Ridha,Lafrenière Ronald G.,Lacaille Jean-Claude,Mottron Laurent,Drapeau Pierre,Beauchamp Miriam H.,Phillips Michael S.,Fombonne Eric,Rouleau Guy A.,Michaud Jacques L.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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4. Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X;Haesler;PLoS Biol.,2007

5. Human-specific transcriptional regulation of CNS development genes by FOXP2;Konopka;Nature,2009

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