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3. 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]
4. 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]
5. 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]
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9. Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1). Aldred MJ; Crawford PJ; Roberts E; Thomas NS Hum Genet; 1992 Dec; 90(4):413-6. PubMed ID: 1483698 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Polymorphism (g2035C>T) in the amelogenin gene. Hart PS; Vlaservich AC; Hart TC; Wright JT Hum Mutat; 2000 Mar; 15(3):298. PubMed ID: 10679955 [No Abstract] [Full Text] [Related]
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17. Novel FAM20A mutations in hypoplastic amelogenesis imperfecta. Cho SH; Seymen F; Lee KE; Lee SK; Kweon YS; Kim KJ; Jung SE; Song SJ; Yildirim M; Bayram M; Tuna EB; Gencay K; Kim JW Hum Mutat; 2012 Jan; 33(1):91-4. PubMed ID: 21990045 [TBL] [Abstract][Full Text] [Related]
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