We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleWDR35 mutation in siblings with Sensenbrenner syndrome: a ciliopathy with variable phenotype.AuthorsBacino CA; Dhar SU; Brunetti-Pierri N; Lee B; Bonnen PEPublicationAmerican journal of medical genetics. Part A, 2012, Vol 158A, Issue 11, p2917ISSN1552-4833Publication typearticleDOI10.1002/ajmg.a.35608