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28. Understanding enamel formation from mutations causing X-linked amelogenesis imperfecta. Lagerström-Fermér M; Landegren U Connect Tissue Res; 1995; 32(1-4):241-6. PubMed ID: 7554922 [No Abstract] [Full Text] [Related]
29. [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]
30. 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]
32. 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]
33. A multidisciplinary approach for the diagnosis of hypocalcified amelogenesis imperfecta in two Chilean families. Urzúa B; Ortega-Pinto A; Farias DA; Franco E; Morales-Bozo I; Moncada G; Escobar-Pezoa N; Scholz U; Cifuentes V Acta Odontol Scand; 2012 Jan; 70(1):7-14. PubMed ID: 21504268 [TBL] [Abstract][Full Text] [Related]
34. [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]
35. Genetic heterogeneity of autosomal dominant amelogenesis imperfecta demonstrated by its exclusion from the AIH2 region on human chromosome 4Q. Kärrman C; Bäckman B; Holmgren G; Forsman K Arch Oral Biol; 1996; 41(8-9):893-900. PubMed ID: 9022927 [TBL] [Abstract][Full Text] [Related]
36. 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]
37. Microradiographic study of amelogenesis imperfecta. Bäckman B; Anneroth G Scand J Dent Res; 1989 Aug; 97(4):316-29. PubMed ID: 2799270 [TBL] [Abstract][Full Text] [Related]