These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
102 related articles for article (PubMed ID: 5280926)
21. Genetic variation and tooth development. Sofaer JA Br Med Bull; 1975 May; 31(2):107-10. PubMed ID: 1100163 [No Abstract] [Full Text] [Related]
22. [Amelogenesis imperfecta (clinical case and discussion)]. Preda GE; Zanasi G; Ricotti E Riv Ital Stomatol; 1983 Nov; 52(11):891-6. PubMed ID: 6592718 [No Abstract] [Full Text] [Related]
23. Four cases of inherited enamel hypoplasia. Neiburger EJ Gen Dent; 1990; 38(1):46-8. PubMed ID: 2376319 [No Abstract] [Full Text] [Related]
24. The incidence of enamel hypoplasia in the dental office. Ruprecht A; Batniji S; El-Neweihi E J Can Dent Assoc; 1984 Dec; 50(12):900-2. PubMed ID: 6391631 [No Abstract] [Full Text] [Related]
25. A novel de novo mutation in LAMB3 causes localized hypoplastic enamel in the molar region. Kim YJ; Shin TJ; Hyun HK; Lee SH; Lee ZH; Kim JW Eur J Oral Sci; 2016 Aug; 124(4):403-5. PubMed ID: 27220909 [TBL] [Abstract][Full Text] [Related]
27. Hereditary enamel hypoplasia in a prehistoric Indian child. Cook DC J Dent Res; 1980 Sep; 59(9):1522. PubMed ID: 6995509 [No Abstract] [Full Text] [Related]
28. Oral rehabilitation of young adults with amelogenesis imperfecta. Yip HK; Smales RJ Int J Prosthodont; 2003; 16(4):345-9. PubMed ID: 12956485 [TBL] [Abstract][Full Text] [Related]
29. Generalized enamel hypoplasia and renal dysfunction. MacGibbon D Aust Dent J; 1972 Feb; 17(1):61-3. PubMed ID: 4504766 [No Abstract] [Full Text] [Related]
30. Unraveling the science of tooth enamel. Bonett JB Penn Dent J (Phila); 2005; ():6-9. PubMed ID: 16173233 [No Abstract] [Full Text] [Related]
31. Enamel formation and amelogenesis imperfecta. Hu JC; Chun YH; Al Hazzazzi T; Simmer JP Cells Tissues Organs; 2007; 186(1):78-85. PubMed ID: 17627121 [TBL] [Abstract][Full Text] [Related]
32. Candidate gene strategy reveals ENAM mutations. Kang HY; Seymen F; Lee SK; Yildirim M; Tuna EB; Patir A; Lee KE; Kim JW J Dent Res; 2009 Mar; 88(3):266-9. PubMed ID: 19329462 [TBL] [Abstract][Full Text] [Related]
33. Hereditary and idiopathic anomalies of tooth number, structure and form. Winter GB Dent Clin North Am; 1969 Apr; 13(2):355-73. PubMed ID: 5251329 [No Abstract] [Full Text] [Related]
34. Relationship of phenotype and genotype in X-linked amelogenesis imperfecta. Wright JT; Hart PS; Aldred MJ; Seow K; Crawford PJ; Hong SP; Gibson CW; Hart TC Connect Tissue Res; 2003; 44 Suppl 1():72-8. PubMed ID: 12952177 [TBL] [Abstract][Full Text] [Related]
35. Amelogenesis imperfecta: a case report. Ogunyinka A West Afr J Med; 2001; 20(1):61-4. PubMed ID: 11505891 [TBL] [Abstract][Full Text] [Related]
36. [Clinical report on a case of amelogenesis imperfecta]. Yoshida T; Minegishi H; Osaka N; Irie E; Kurihara J; Goto H Josai Shika Daigaku Kiyo; 1981; 10(2):315-21. PubMed ID: 6959664 [No Abstract] [Full Text] [Related]
37. Identification of a novel FAM83H mutation and microhardness of an affected molar in autosomal dominant hypocalcified amelogenesis imperfecta. Hyun HK; Lee SK; Lee KE; Kang HY; Kim EJ; Choung PH; Kim JW Int Endod J; 2009 Nov; 42(11):1039-43. PubMed ID: 19825039 [TBL] [Abstract][Full Text] [Related]
38. A conservative treatment for amelogenesis imperfecta with direct resin composite restorations: a case report. Sabatini C; Guzmán-Armstrong S J Esthet Restor Dent; 2009; 21(3):161-9; discussion 170. PubMed ID: 19508258 [TBL] [Abstract][Full Text] [Related]