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 CPublicationOrthodontics & craniofacial research, 2006, Vol 9, Issue 3, p129ISSN1601-6335Publication typearticleDOI10.1111/j.1601-6343.2006.00367.x