Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleA HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndrome.AuthorsInnis, Jeffrey W.; Goodman, Frances R.; Bacchelli, Chiara; Williams, Thomas M.; Mortlock, Douglas P.; Sateesh, Praveen; Scambler, Peter J.; McKinnon, Wendy; Guttmacher, Alan E.PublicationHuman Mutation, 2002, Vol 19, Issue 5, p573ISSN1059-7794Publication typeArticleDOI10.1002/humu.9036