We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.AuthorsKoolen DA; Kramer JM; Neveling K; Nillesen WM; Moore-Barton HL; Elmslie FV; Toutain A; Amiel J; Malan V; Tsai AC; Cheung SW; Gilissen C; Verwiel ET; Martens S; Feuth T; Bongers EM; de Vries P; Scheffer H; Vissers LE; de Brouwer AP; Brunner HG; Veltman JA; Schenck A; Yntema HG; de Vries BBPublicationNature genetics, 2012, Vol 44, Issue 6, p639ISSN1546-1718Publication typearticleDOI10.1038/ng.2262