Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleHigh-Resolution genomic arrays identify CNVs that phenocopy the chromosome 22q11.2 deletion syndrome.AuthorsBusse, Tracy; Graham, John M.; Feldman, Gerald; Perin, Juan; Catherwood, Anne; Knowlton, Robert; Rappaport, Eric F.; Emanuel, Beverly; Driscoll, Deborah A.; Saitta, Sulagna C.PublicationHuman Mutation, 2011, Vol 32, Issue 1, p91ISSN1059-7794Publication typeArticleDOI10.1002/humu.21395