We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleSevere digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13AuthorsDebeer, P.; Bacchelli, C.; Scambler, P.J.; Smet, L. de; Fryns, J-P.; Goodman, F.R.PublicationJournal of Medical Genetics (JMG), 2002, Vol 39, Issue 11, p852ISSN0022-2593Publication typearticle