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23. 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]
24. A novel AMELX mutation causes hypoplastic amelogenesis imperfecta. Kim YJ; Kim YJ; Kang J; Shin TJ; Hyun HK; Lee SH; Lee ZH; Kim JW Arch Oral Biol; 2017 Apr; 76():61-65. PubMed ID: 28130977 [TBL] [Abstract][Full Text] [Related]
25. A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1). Lagerström M; Dahl N; Nakahori Y; Nakagome Y; Bäckman B; Landegren U; Pettersson U Genomics; 1991 Aug; 10(4):971-5. PubMed ID: 1916828 [TBL] [Abstract][Full Text] [Related]
26. Genes and related proteins involved in amelogenesis imperfecta. Stephanopoulos G; Garefalaki ME; Lyroudia K J Dent Res; 2005 Dec; 84(12):1117-26. PubMed ID: 16304440 [TBL] [Abstract][Full Text] [Related]
28. 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]
29. Amelogenin signal peptide mutation: correlation between mutations in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfecta. Lagerström-Fermér M; Nilsson M; Bäckman B; Salido E; Shapiro L; Pettersson U; Landegren U Genomics; 1995 Mar; 26(1):159-62. PubMed ID: 7782077 [TBL] [Abstract][Full Text] [Related]
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34. Splicing mutations in AMELX and ENAM cause amelogenesis imperfecta. Zhang Z; Zou X; Feng L; Huang Y; Chen F; Sun K; Song Y; Lv P; Gao X; Dong Y; Tian H BMC Oral Health; 2023 Nov; 23(1):893. PubMed ID: 37985977 [TBL] [Abstract][Full Text] [Related]
35. Molecular basis and consequences of a deletion in the amelogenin gene, analyzed by capture PCR. Lagerström-Fermér M; Pettersson U; Landegren U Genomics; 1993 Jul; 17(1):89-92. PubMed ID: 8406474 [TBL] [Abstract][Full Text] [Related]
36. SSCP detection of a nonsense mutation in exon 5 of the amelogenin gene (AMGX) causing X-linked amelogenesis imperfecta (AIH1). Lench NJ; Brook AH; Winter GB Hum Mol Genet; 1994 May; 3(5):827-8. PubMed ID: 8081371 [No Abstract] [Full Text] [Related]
37. Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects. Hart TC; Hart PS; Gorry MC; Michalec MD; Ryu OH; Uygur C; Ozdemir D; Firatli S; Aren G; Firatli E J Med Genet; 2003 Dec; 40(12):900-6. PubMed ID: 14684688 [TBL] [Abstract][Full Text] [Related]
38. Phenotypic diversity and revision of the nomenclature for autosomal recessive amelogenesis imperfecta. Nusier M; Yassin O; Hart TC; Samimi A; Wright JT Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2004 Feb; 97(2):220-30. PubMed ID: 14970781 [TBL] [Abstract][Full Text] [Related]
39. Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta. Santos MC; Hart PS; Ramaswami M; Kanno CM; Hart TC; Line SR Head Face Med; 2007 Jan; 3():8. PubMed ID: 17266769 [TBL] [Abstract][Full Text] [Related]