Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE
Celestino-Soper PB, Shaw CA, Sanders SJ, Li J, Murtha MT, Ercan-Sencicek AG, Davis L, Thomson S, Gambin T, Chinault AC, Ou Z, German JR, Milosavljevic A, Sutcliffe JS, Cook EH, Stankiewicz P, State MW, Beaudet AL. Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE. Human Molecular Genetics 2011, 20: 4360-4370. PMID: 21865298, PMCID: PMC3196886, DOI: 10.1093/hmg/ddr363.Peer-Reviewed Original ResearchMeSH KeywordsAutistic DisorderComparative Genomic HybridizationDNA Copy Number VariationsExonsFemaleHumansMaleMixed Function OxygenasesConceptsCopy number variantsSingle protein-coding geneProtein-coding genesNumber variantsSingle nucleotide polymorphism arrayArray comparative genomic hybridizationExonic copy number variantsSmall copy number variantsComparative genomic hybridizationFirst enzymeUnique exonsX chromosomeRefSeq genesGenomic variantsHeterogeneous genetic etiologyOligonucleotide arraysPolymorphism arrayIndividual B cellsClonal outgrowthAutism familiesExonic deletionsGenomic hybridizationSimons Simplex CollectionHemizygous deletionSomatic mutations