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Results: 2
XLID-Causing Mutations and Associated Genes Challenged in Light of Data From Large-Scale Human Exome Sequencing
Authors: Piton, Amélie Redin, Claire Mandel, Jean-Louis
Citation: Piton, Amélie et al., XLID-Causing Mutations and Associated Genes Challenged in Light of Data From Large-Scale Human Exome Sequencing, American journal of human genetics (Online) AJHG , 93(2), 2013, pp. 368-383
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
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
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