Open AccessPathogenic copy number variants (pCNVs) in individuals diagnosed on the autism spectrum disorder (ASD): A closer look at candidate genes
Author(s) -
Allan Dale Baniaga
Publication year - 2011
Publication title -
mcgill science undergraduate research journal
Language(s) - English
Resource type - Journals
eISSN - 1718-0783
pISSN - 1718-0775
DOI - 10.26443/msurj.v6i1.89
Subject(s) - autism , copy number variation , candidate gene , geneticist , phenotype , comparative genomic hybridization , genetics , gene , gene duplication , autism spectrum disorder , biology , bioinformatics , medicine , genome , psychiatry
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