Authors:
Hamdan, Fadi F.
Daoud, Hussein
Rochefort, Daniel
Piton, Amélie
Michaud, Jacques L.
Citation: F. Hamdan, Fadi et al., De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language ImpairmentDe Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment, American journal of human genetics (Online) AJHG , 87(5), 2010, pp. 671-678