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.
23. Scanning electron microscopic study of hypoplastic type amelogenesis imperfecta in primary teeth. Uzamis M; Celik H; Erkmen N; Batirbaygil Y J Clin Pediatr Dent; 1997; 21(3):265-8. PubMed ID: 9484138 [TBL] [Abstract][Full Text] [Related]
24. Epidemiology of enamel hypoplasia in deciduous teeth: explaining variation in prevalence in western India. Lukacs JR; Walimbe SR; Floyd B Am J Hum Biol; 2001; 13(6):788-807. PubMed ID: 11748818 [TBL] [Abstract][Full Text] [Related]
25. The mineral composition and enamel ultrastructure of hypocalcified amelogenesis imperfecta. Wright JT; Duggal MS; Robinson C; Kirkham J; Shore R J Craniofac Genet Dev Biol; 1993; 13(2):117-26. PubMed ID: 8325967 [TBL] [Abstract][Full Text] [Related]
26. Hereditary amelogenesis imperfecta. I. Epidemiology and clinical classification in a Swedish child population. Sundell S; Koch G Swed Dent J; 1985; 9(4):157-69. PubMed ID: 3864268 [TBL] [Abstract][Full Text] [Related]
27. [A case of systemic hypomineralization of the enamel]. Hanzély B Fogorv Sz; 1971 May; 64(5):150-3. PubMed ID: 5280926 [No Abstract] [Full Text] [Related]
28. Enamel hypoplasia in the middle pleistocene hominids from Atapuerca (Spain). Bermúdez de Castro JM; Pérez PJ Am J Phys Anthropol; 1995 Mar; 96(3):301-14. PubMed ID: 7785727 [TBL] [Abstract][Full Text] [Related]
29. Diagnosis of enamel defects. Sarnat H; Moss SJ N Y State Dent J; 1985 Feb; 51(2):103-4, 106. PubMed ID: 3856783 [No Abstract] [Full Text] [Related]
30. [A familial strain of amelogenesis imperfecta hypoplastic type with dominant x-linked heredity]. Cassese M; Grulliero A; Di Napoli G; Ventruto V Minerva Stomatol; 1976; 25(2):89-94. PubMed ID: 1069908 [TBL] [Abstract][Full Text] [Related]
32. Dental enamel formation and its impact on clinical dentistry. Simmer JP; Hu JC J Dent Educ; 2001 Sep; 65(9):896-905. PubMed ID: 11569606 [TBL] [Abstract][Full Text] [Related]
33. Localization of a gene for autosomal dominant amelogenesis imperfecta (ADAI) to chromosome 4q. Forsman K; Lind L; Bäckman B; Westermark E; Holmgren G Hum Mol Genet; 1994 Sep; 3(9):1621-5. PubMed ID: 7833920 [TBL] [Abstract][Full Text] [Related]
34. Factors affecting the distribution of enamel hypoplasias within the human permanent dentition. Goodman AH; Armelagos GJ Am J Phys Anthropol; 1985 Dec; 68(4):479-93. PubMed ID: 3909823 [TBL] [Abstract][Full Text] [Related]
35. 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]
37. [A clinical study of traumatic injuries to deciduous teeth. (3). The influence on their permanent successors]. Ishikawa M; Satoh K; Miyashin M Shoni Shikagaku Zasshi; 1990; 28(2):397-406. PubMed ID: 2133949 [TBL] [Abstract][Full Text] [Related]
38. [Amelogenesis imperfecta and hypothalamo-hypophyseal insufficiency]. Ajacques JC; David M; Farge P Rev Stomatol Chir Maxillofac; 1989; 90(4):253-8. PubMed ID: 2762743 [TBL] [Abstract][Full Text] [Related]
39. [Clinical study of enamel hypoplasia and its causes. 1. Primary teeth]. Nozaka K; Sato T; Mukaida T; Shimazu A; Hasegawa J; Amari E Shoni Shikagaku Zasshi; 1990; 28(3):561-78. PubMed ID: 2133959 [TBL] [Abstract][Full Text] [Related]
40. [Genetic defects of the enamel]. Skrinjarić I Acta Stomatol Croat; 1985; 19(1):57-67. PubMed ID: 3859996 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]