Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleX-linked VACTERL with hydrocephalus syndrome: Further delineation of the phenotype caused by FANCB mutations.AuthorsMcCauley, Joanna; Masand, Navta; McGowan, Ruth; Rajagopalan, Sulekha; Hunter, Alasdair; Michaud, Jacques L.; Gibson, Kate; Robertson, Jeremy; Vaz, Fiona; Abbs, Stephen; Holden, Simon T.PublicationAmerican Journal of Medical Genetics. Part A, 2011, Vol 155A, Issue 10, p2370ISSN1552-4825Publication typeArticleDOI10.1002/ajmg.a.33913