We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleA new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.AuthorsKoolen DA; Vissers LE; Pfundt R; de Leeuw N; Knight SJ; Regan R; Kooy RF; Reyniers E; Romano C; Fichera M; Schinzel A; Baumer A; Anderlid BM; Schoumans J; Knoers NV; van Kessel AG; Sistermans EA; Veltman JA; Brunner HG; de Vries BBPublicationNature genetics, 2006, Vol 38, Issue 9, p999ISSN1061-4036Publication typearticleDOI10.1038/ng1853