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2. Enamelin (Enam) is essential for amelogenesis: ENU-induced mouse mutants as models for different clinical subtypes of human amelogenesis imperfecta (AI). Masuya H; Shimizu K; Sezutsu H; Sakuraba Y; Nagano J; Shimizu A; Fujimoto N; Kawai A; Miura I; Kaneda H; Kobayashi K; Ishijima J; Maeda T; Gondo Y; Noda T; Wakana S; Shiroishi T Hum Mol Genet; 2005 Mar; 14(5):575-83. PubMed ID: 15649948 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Unraveling the science of tooth enamel. Bonett JB Penn Dent J (Phila); 2005; ():6-9. PubMed ID: 16173233 [No Abstract] [Full Text] [Related]
5. Enamel formation and amelogenesis imperfecta. Hu JC; Chun YH; Al Hazzazzi T; Simmer JP Cells Tissues Organs; 2007; 186(1):78-85. PubMed ID: 17627121 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. The structure and composition of deciduous enamel affected by local hypoplastic autosomal dominant amelogenesis imperfecta resulting from an ENAM mutation. Shore RC; Bäckman B; Elcock C; Brook AH; Brookes SJ; Kirkham J Cells Tissues Organs; 2010; 191(4):301-6. PubMed ID: 19923784 [TBL] [Abstract][Full Text] [Related]
9. [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]
10. 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]
11. PCR detection of the human amelogenin gene and its application to the diagnosis of amelogenesis imperfecta. Sekiguchi H; Minaguchi K; Machida Y; Yakushiji M Bull Tokyo Dent Coll; 1998 Nov; 39(4):275-85. PubMed ID: 10218009 [TBL] [Abstract][Full Text] [Related]
12. Human enamel phenotype associated with amelogenesis imperfecta and a kallikrein-4 (g.2142G>A) proteinase mutation. Wright JT; Daly B; Simmons D; Hong S; Hart SP; Hart TC; Atsawasuwan P; Yamauchi M Eur J Oral Sci; 2006 May; 114 Suppl 1():13-7; discussion 39-41, 379. PubMed ID: 16674656 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Amelogenesis imperfecta, a new dental mutation in rats. Ishibashi K; Iino T; Sekiguchi F Lab Anim Sci; 1990 Jan; 40(1):16-20. PubMed ID: 2153852 [TBL] [Abstract][Full Text] [Related]