Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleRare mutations of FGFR2 causing apert syndrome: identification of the first partial gene deletion, and an Alu element insertion from a new subfamily.AuthorsBochukova, Elena G.; Roscioli, Tony; Hedges, Dale J.; Taylor, Indira B.; Johnson, David; David, David J.; Deininger, Prescott L.; Wilkie, Andrew O.M.PublicationHuman Mutation, 2009, Vol 30, Issue 2, p204ISSN1059-7794Publication typeArticleDOI10.1002/humu.20825