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12. Dentinogenesis imperfecta type II: an affected family saga. Kamboj M; Chandra A J Oral Sci; 2007 Sep; 49(3):241-4. PubMed ID: 17928732 [TBL] [Abstract][Full Text] [Related]
13. Dentinogenesis imperfecta in a six-generation family. A clinical, radiographic and histologic comparison of two branches through three generations. Malmgren B; Lundberg M; Lindskog S Swed Dent J; 1988; 12(3):73-84. PubMed ID: 3165569 [TBL] [Abstract][Full Text] [Related]
14. [Clinical and genetic study of hereditary dentinogenesis imperfecta]. Velley J Actual Odontostomatol (Paris); 1974 Sep; (107):519-32. PubMed ID: 4455066 [No Abstract] [Full Text] [Related]
16. [Capdepont dysplasia and vertical excess of the lower half of the face. Genetic syndrome or fortuitous association?]. Deffez JP; Rostand B; Brethaux J; Allain P; Hazen M Rev Stomatol Chir Maxillofac; 1986; 87(3):131-7. PubMed ID: 3464066 [TBL] [Abstract][Full Text] [Related]
17. Dentinogenesis imperfecta traceable through five generations of a part American Indian family. Miller WA; Winkler S; Rosenberg JJ; Mastracola R; Fischman SL; Wolfe RJ Oral Surg Oral Med Oral Pathol; 1973 Feb; 35(2):180-6. PubMed ID: 4513064 [No Abstract] [Full Text] [Related]
18. [Hereditary pathology of the enamel and dentin. A review of molecular genetic research]. Beliakov IuA; Elizarova VM; Krotov VA; Blinnikova OE Stomatologiia (Mosk); 2000; 79(1):8-9. PubMed ID: 10693338 [TBL] [Abstract][Full Text] [Related]
19. [Family tree and restoration method of hereditary opalescent dentin: a case report]. Zhou P; Wang ZS; Xu HZ; Li YF Hua Xi Kou Qiang Yi Xue Za Zhi; 2009 Oct; 27(5):574-6. PubMed ID: 19927739 [TBL] [Abstract][Full Text] [Related]