Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders

Copy number variants (CNVs) have repeatedly been found to cause or predispose to autism spectrum disorders (ASDs). For diagnostic purposes, we screened 194 individuals with ASDs for CNVs using Illumina SNP arrays. In several probands, we also analyzed candidate genes located in inherited deletions t...

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Main Authors: Nava, Caroline, Keren, Boris, Mignot, Cyril, Rastetter, Agnès, Chantot-Bastaraud, Sandra, Faudet, Anne, Fonteneau, Eric, Amiet, Claire, Laurent, Claudine, Jacquette, Aurélia, Whalen, Sandra, Afenjar, Alexandra, Périsse, Didier, Doummar, Diane, Dorison, Nathalie, Leboyer, Marion, Siffroi, Jean-Pierre, Cohen, David, Brice, Alexis, Héron, Delphine, Depienne, Christel
Formáid: Artigo
Teanga:Inglês
Foilsithe: Nature Publishing Group 2014
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Article
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3865413/
https://ncbi.nlm.nih.gov/pubmed/23632794
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2013.88
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