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2. 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]
3. Craniofacial structure related to inheritance pattern in amelogenesis imperfecta. Bäckman B; Adolfsson U Am J Orthod Dentofacial Orthop; 1994 Jun; 105(6):575-82. PubMed ID: 8198082 [TBL] [Abstract][Full Text] [Related]
4. [A particular type of dominant hereditary enamel dysplasia?]. Weyers H Dtsch Zahnarztl Z; 1977 Mar; 32(3):243-7. PubMed ID: 265269 [TBL] [Abstract][Full Text] [Related]
5. [Genetic studies on X-chromosomal, incompletely dominant hypoplasia of tooth enamel]. Kalden M Dtsch Zahnarztl Z; 1988 Nov; 43(11):1177-81. PubMed ID: 3251735 [No Abstract] [Full Text] [Related]
6. Hereditary amelogenesis imperfecta. An epidemiological, genetic and clinical study in a Swedish child population. Sundell S Swed Dent J Suppl; 1986; 31():1-38. PubMed ID: 3460191 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. [Hereditary type enamel hypoplasia. Clinical and histopathological findings of an observed case]. Debernardi C; Pirrello D Minerva Stomatol; 1989 Mar; 38(3):321-34. PubMed ID: 2657367 [TBL] [Abstract][Full Text] [Related]
9. [Regularly dominant autosomal enamel hypoplasia with a frontal open bite: chance or pleiotropy?]. Tammoscheit UG ZWR; 1979 Nov; 88(21):952, 955-6. PubMed ID: 294008 [No Abstract] [Full Text] [Related]
10. Hereditary enamel hypoplasia. Torres-Laz MS J Philipp Dent Assoc; 1998; 50(2):18-21. PubMed ID: 10597144 [No Abstract] [Full Text] [Related]
11. [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]
13. [Changes in the enamel structure of permanent teeth acquired during amelogenesis]. Montagne F Inf Dent; 1985 Apr; 67(15):1417-29. PubMed ID: 3863790 [No Abstract] [Full Text] [Related]
14. Ataxia, mental deterioration, epilepsy in a family with dominant enamel hypoplasia: a variant of Kohlschütter-Tönz syndrome? Guazzi G; Palmeri S; Malandrini A; Ciacci G; Di Perri R; Mancini G; Messina C; Salvadori C Am J Med Genet; 1994 Mar; 50(1):79-83. PubMed ID: 8160757 [TBL] [Abstract][Full Text] [Related]