Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleRefinement of the critical region of 1q41q42 microdeletion syndrome identifies FBXO28 as a candidate causative gene for intellectual disability and seizures.AuthorsAu, P.Y. Billie; Argiropoulos, Bob; Parboosingh, Jillian S.; Micheil Innes, A.PublicationAmerican Journal of Medical Genetics. Part A, 2014, Vol 164A, Issue 2, p441ISSN1552-4825Publication typeArticleDOI10.1002/ajmg.a.36320