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2. Clinical features of a family with X-linked amelogenesis imperfecta mapping to a new locus (AIH3) on the long arm of the X chromosome. Crawford PJ; Aldred MJ Oral Surg Oral Med Oral Pathol; 1993 Aug; 76(2):187-91. PubMed ID: 8361730 [TBL] [Abstract][Full Text] [Related]
3. Enamel ultrastructure and protein content in X-linked amelogenesis imperfecta. Wright JT; Aldred MJ; Crawford PJ; Kirkham J; Robinson C Oral Surg Oral Med Oral Pathol; 1993 Aug; 76(2):192-9. PubMed ID: 8361731 [TBL] [Abstract][Full Text] [Related]
4. X-linked amelogenesis imperfecta. Presentation of two kindreds and a review of the literature. Crawford PJ; Aldred MJ Oral Surg Oral Med Oral Pathol; 1992 Apr; 73(4):449-55. PubMed ID: 1574307 [TBL] [Abstract][Full Text] [Related]
5. Detection of a novel mutation in X-linked amelogenesis imperfecta. Kindelan SA; Brook AH; Gangemi L; Lench N; Wong FS; Fearne J; Jackson Z; Foster G; Stringer BM J Dent Res; 2000 Dec; 79(12):1978-82. PubMed ID: 11201048 [TBL] [Abstract][Full Text] [Related]
12. Hypomaturation amelogenesis imperfecta: account of a family with an X-linked inheritance pattern. Bundzman ER; Modesto A Braz Dent J; 1999; 10(2):111-6. PubMed ID: 10863398 [TBL] [Abstract][Full Text] [Related]
13. Limited phenotypic variation of hypocalcified amelogenesis imperfecta in a Danish five-generation family with a novel FAM83H nonsense mutation. Haubek D; Gjørup H; Jensen LG; Juncker I; Nyegaard M; Børglum AD; Poulsen S; Hertz JM Int J Paediatr Dent; 2011 Nov; 21(6):407-12. PubMed ID: 21702852 [TBL] [Abstract][Full Text] [Related]
14. Local, hypoplastic type of amelogenesis imperfecta: a clinical, genetic, radiological and dermatoglyphic study. Atasu M; Genc A; Namdar F J Clin Pediatr Dent; 1996; 20(4):337-42. PubMed ID: 9151630 [TBL] [Abstract][Full Text] [Related]
16. [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]
17. 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]
18. 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]
19. Amelogenesis imperfecta with taurodontism. Congleton J; Burkes EJ Oral Surg Oral Med Oral Pathol; 1979 Dec; 48(6):540-4. PubMed ID: 292959 [TBL] [Abstract][Full Text] [Related]