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2. 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]
3. [Amelogenesis imperfecta in the lower dentition of an 8-year-old girl]. Bakody R; Simon Z Fogorv Sz; 1986 Apr; 79(4):118-9. PubMed ID: 3457714 [No Abstract] [Full Text] [Related]
4. A new classification of heritable human enamel defects and a discussion of dentin defects. Shields ED Birth Defects Orig Artic Ser; 1983; 19(1):107-27. PubMed ID: 6362739 [TBL] [Abstract][Full Text] [Related]
5. The treatment of hypoplastic and hypomineralised teeth. Andlaw RJ Proc Br Paedod Soc; 1983; 13():25-30. PubMed ID: 6591174 [No Abstract] [Full Text] [Related]
6. 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]
7. [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]
8. 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]
9. The effects of acid-etching on enamel from different clinical variants of amelogenesis imperfecta: an SEM study. Seow WK; Amaratunge A Pediatr Dent; 1998; 20(1):37-42. PubMed ID: 9524971 [TBL] [Abstract][Full Text] [Related]
10. [A case report of hereditary amelogenesis imperfecta in a family (author's transl)]. Minegishi H; Irie E; Osaka N; Moriyama K; Sano M; Ito H; Hamamoto Y; Goto H Josai Shika Daigaku Kiyo; 1979; 8(3):413-7. PubMed ID: 297513 [No Abstract] [Full Text] [Related]
11. Ultrastructural study of tooth enamel with amelogenesis imperfecta in AI-nephrocalcinosis syndrome. Phakey P; Palamara J; Hall RK; McCredie DA Connect Tissue Res; 1995; 32(1-4):253-9. PubMed ID: 7554924 [TBL] [Abstract][Full Text] [Related]
12. Hereditary amelogenesis imperfecta. A rare autosomal dominant type. Winter GB; Lee KW; Johnson NW Br Dent J; 1969 Aug; 127(4):157-64. PubMed ID: 5258202 [No Abstract] [Full Text] [Related]
13. 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]
14. Enamel hypoplasia and anomalies of the enamel. Winter GB; Brook AH Dent Clin North Am; 1975 Jan; 19(1):3-24. PubMed ID: 162891 [No Abstract] [Full Text] [Related]
15. Amelogenesis imperfecta: diagnosis and resolution of a case with hypoplasia and hypocalcification of enamel, dental agenesis, and skeletal open bite. Pulgar Encinas R; García-Espona I; Navajas Rodriguez de Mondelo JM Quintessence Int; 2001 Mar; 32(3):183-9. PubMed ID: 12066657 [TBL] [Abstract][Full Text] [Related]
16. [An enamel disorder in two siblings]. Créton MA; Cune MS Ned Tijdschr Tandheelkd; 2004 Oct; 111(10):400-2. PubMed ID: 15553370 [TBL] [Abstract][Full Text] [Related]
17. [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]
18. [A critical study of amelogenesis imperfecta]. Kerebel B; Dubois T Bull Group Int Rech Sci Stomatol Odontol; 1982 Dec; 25(4):291-311. PubMed ID: 6961948 [No Abstract] [Full Text] [Related]