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24. [Prosthetic management in a case of hereditary dentinogenesis imperfecta]. Stós B; Szukiel A Protet Stomatol; 1983; 33(3):187-91. PubMed ID: 6585865 [No Abstract] [Full Text] [Related]
25. Dentinogenesis Inperfecta. Report of three cases in an Indian family. Raji MA; Vargheese NO; Grorge K Indian J Dent Res; 1993; 4(2):59-64. PubMed ID: 8180285 [TBL] [Abstract][Full Text] [Related]
26. Treatment of dentinogenesis imperfecta in a child: report of case. Nayar AK; Latta JB; Soni NN ASDC J Dent Child; 1981; 48(6):453-5. PubMed ID: 6946089 [No Abstract] [Full Text] [Related]
30. [Clinical picture, histological demonstration and prosthetic treatment of a case of dentinogenesis imperfecta]. Gyimesi J Dtsch Zahnarztl Z; 1970; 25(7):748-51. PubMed ID: 5269706 [No Abstract] [Full Text] [Related]
31. 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; 51(5):383-408. PubMed ID: 18599376 [TBL] [Abstract][Full Text] [Related]
32. Genomic organization of the human osteopontin gene: exclusion of the locus from a causative role in the pathogenesis of dentinogenesis imperfecta type II. Crosby AH; Edwards SJ; Murray JC; Dixon MJ Genomics; 1995 May; 27(1):155-60. PubMed ID: 7665163 [TBL] [Abstract][Full Text] [Related]
33. [Imperfect among the imperfect--dentinogenesis. Not always are all the pecularities of a disease present]. De Ulnik MG Fauchard; 1970 Aug; 1(8):358-60. PubMed ID: 5283177 [No Abstract] [Full Text] [Related]
34. Elucidation of the sequence and the genomic organization of the human dentin matrix acidic phosphoprotein 1 (DMP1) gene: exclusion of the locus from a causative role in the pathogenesis of dentinogenesis imperfecta type II. Hirst KL; Simmons D; Feng J; Aplin H; Dixon MJ; MacDougall M Genomics; 1997 May; 42(1):38-45. PubMed ID: 9177774 [TBL] [Abstract][Full Text] [Related]
36. Mapping of the human dentin matrix acidic phosphoprotein gene (DMP1) to the dentinogenesis imperfecta type II critical region at chromosome 4q21. Aplin HM; Hirst KL; Crosby AH; Dixon MJ Genomics; 1995 Nov; 30(2):347-9. PubMed ID: 8586437 [TBL] [Abstract][Full Text] [Related]
37. Heritable dentin defects: nosology, pathology, and treatment. Ranta H; Lukinmaa PL; Waltimo J Am J Med Genet; 1993 Jan; 45(2):193-200. PubMed ID: 8456802 [TBL] [Abstract][Full Text] [Related]