1. WNT10A mutations account for ¼ of population-based isolated oligodontia and show phenotypic correlations;Arzoo;Am J Med Genet A,2014
2. Development and evaluation of a comprehensive screening for orofacial dysfunction;Bakke;Swed Dent J,2007
3. Oligodontia and ectodermal dysplasia-on signs, symptoms, genetics, and outcomes of dental treatment;Bergendal;Swed Dent J,2010
4. Signs and symptoms from ectodermal organs in young Swedish individuals with oligodontia;Bergendal;Int J Paediatr Dent,2006
5. Comprehensive Treatment Planning for the Patient with Complex Treatment Needs