Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleExome sequencing identifies a novel EP300 frame shift mutation in a patient with features that overlap cornelia de lange syndrome.AuthorsWoods, Susan A.; Robinson, Haynes B.; Kohler, Lisa J.; Agamanolis, Dimitris; Sterbenz, George; Khalifa, MohamedPublicationAmerican Journal of Medical Genetics. Part A, 2014, Vol 164A, Issue 1, p251ISSN1552-4825Publication typeArticleDOI10.1002/ajmg.a.36237