We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleExclusion of coding region mutations in MSX1, PAX9 and AXIN2 in eight patients with severe oligodontia phenotype.AuthorsGerits, A; Nieminen, P; De Muynck, S; Carels, CAbstractThis paper describes the screening of eight patients with severe oligodontia for PAX9 and AXIN2 mutations.PublicationOrthodontics & craniofacial research, 2006, Vol 9, Issue 3, p129ISSN1601-6335Publication typeJournal ArticleDOI10.1111/j.1601-6343.2006.00367.x