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
Hum Mol Genet. 2011 20 (22): 4360-70

PMID: 21865298 · PMCID: PMC3196886 · DOI:10.1093/hmg/ddr363

MeSH Terms (8)

Autistic Disorder Comparative Genomic Hybridization DNA Copy Number Variations Exons Female Humans Male Mixed Function Oxygenases

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