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43. Frameshift mutations in dentin phosphoprotein and dependence of dentin disease phenotype on mutation location. Nieminen P; Papagiannoulis-Lascarides L; Waltimo-Siren J; Ollila P; Karjalainen S; Arte S; Veerkamp J; Tallon Walton V; Chimenos Küstner E; Siltanen T; Holappa H; Lukinmaa PL; Alaluusua S J Bone Miner Res; 2011 Apr; 26(4):873-80. PubMed ID: 20949630 [TBL] [Abstract][Full Text] [Related]
44. [Pedigree analysis and prosthodontic treatment of patients with dentinogenesis imperfecta type II]. Gan H; Zhang XY; Xu XC Shanghai Kou Qiang Yi Xue; 2009 Aug; 18(4):337-41. PubMed ID: 19760002 [TBL] [Abstract][Full Text] [Related]
45. Splicing site mutations in dentin sialophosphoprotein causing dentinogenesis imperfecta type II. Holappa H; Nieminen P; Tolva L; Lukinmaa PL; Alaluusua S Eur J Oral Sci; 2006 Oct; 114(5):381-4. PubMed ID: 17026502 [TBL] [Abstract][Full Text] [Related]
46. Novel dentin phosphoprotein frameshift mutations in dentinogenesis imperfecta type II. Lee KE; Kang HY; Lee SK; Yoo SH; Lee JC; Hwang YH; Nam KH; Kim JS; Park JC; Kim JW Clin Genet; 2011 Apr; 79(4):378-84. PubMed ID: 20618350 [TBL] [Abstract][Full Text] [Related]
47. SEM-morphology in dentinogenesis imperfecta type II: microscopic anatomy and efficacy of a dentine bonding system. Gallusi G; Libonati A; Campanella V Eur J Paediatr Dent; 2006 Mar; 7(1):9-17. PubMed ID: 16646639 [TBL] [Abstract][Full Text] [Related]
48. Amelogenesis imperfecta with taurodontism and the tricho-dento-osseous syndrome: separate conditions or a spectrum of disease? Crawford PJ; Aldred MJ Clin Genet; 1990 Jul; 38(1):44-50. PubMed ID: 2387085 [TBL] [Abstract][Full Text] [Related]
49. 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]
50. Oral findings in osteogenesis imperfecta. Schwartz S; Tsipouras P Oral Surg Oral Med Oral Pathol; 1984 Feb; 57(2):161-7. PubMed ID: 6583624 [TBL] [Abstract][Full Text] [Related]
51. Dentinogenesis imperfecta: a case report. Mayordomo FG; Estrela F; de Aldecoa EA Quintessence Int; 1992 Dec; 23(12):795-802. PubMed ID: 1305296 [TBL] [Abstract][Full Text] [Related]
52. An autosomal-dominant form of juvenile periodontitis: its localization to chromosome 4 and linkage to dentinogenesis imperfecta and Gc. Boughman JA; Halloran SL; Roulston D; Schwartz S; Suzuki JB; Weitkamp LR; Wenk RE; Wooten R; Cohen MM J Craniofac Genet Dev Biol; 1986; 6(4):341-50. PubMed ID: 3793857 [TBL] [Abstract][Full Text] [Related]
53. Dentinogenesis imperfecta in children with osteogenesis imperfecta: a clinical and ultrastructural study. Majorana A; Bardellini E; Brunelli PC; Lacaita M; Cazzolla AP; Favia G Int J Paediatr Dent; 2010 Mar; 20(2):112-8. PubMed ID: 20384825 [TBL] [Abstract][Full Text] [Related]
54. 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]
55. A probable common disturbance in the early stage of odontoblast differentiation in Dentinogenesis imperfecta type I and type II. Takagi Y; Sasaki S J Oral Pathol; 1988 May; 17(5):208-12. PubMed ID: 2462619 [TBL] [Abstract][Full Text] [Related]
56. Dental findings in osteogenesis imperfecta: I. Occurrence and expression of type I dentinogenesis imperfecta. Lukinmaa PL; Ranta H; Ranta K; Kaitila I J Craniofac Genet Dev Biol; 1987; 7(2):115-25. PubMed ID: 3624417 [TBL] [Abstract][Full Text] [Related]
60. [Occurrence of dentinogenesis imperfecta hereditaria (Capdepont's disease) in four successive generations of one family]. Szczepanński M; Uścinowicz M; Kaczmarski M Pediatr Pol; 1995 Aug; 70(8):679-81. PubMed ID: 8668371 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]