We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleUse of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE.AuthorsCelestino-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 Jr; Stankiewicz P; State MW; Beaudet ALPublicationHuman molecular genetics, 2011, Vol 20, Issue 22, p4360ISSN1460-2083Publication typearticleDOI10.1093/hmg/ddr363