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13. The genetic basis of inherited anomalies of the teeth. Part 2: syndromes with significant dental involvement. Bailleul-Forestier I, Berdal A, Vinckier F, de Ravel T, Fryns JP, Verloes A. Eur J Med Genet; 2008 Apr; 51(5):383-408. PubMed ID: 18599376 [Abstract] [Full Text] [Related]
20. Familial tarda type osteogenesis imperfecta with dentinogenesis imperfecta Type I. Case report. Ogunsalu C, Hanchard B. Aust Dent J; 1997 Jun; 42(3):175-7. PubMed ID: 9241928 [Abstract] [Full Text] [Related] Page: [Next] [New Search]