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Journal Abstract Search

161 related items for PubMed ID: 8081371

  • 1. 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
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  • 2. Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1).
    Lench NJ, Winter GB.
    Hum Mutat; 1995 May; 5(3):251-9. PubMed ID: 7599636
    [Abstract] [Full Text] [Related]

  • 3. DNA diagnosis of X-linked amelogenesis imperfecta (AIH1).
    Lench NJ, Brook AH.
    J Oral Pathol Med; 1997 Mar; 26(3):135-7. PubMed ID: 9083938
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  • 4. 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
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  • 5. 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
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  • 6. 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 01; 26(1):159-62. PubMed ID: 7782077
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  • 7. 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 01; 10(4):971-5. PubMed ID: 1916828
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  • 13. Molecular analysis for genetic counselling in amelogenesis imperfecta.
    Aldred MJ, Hall RK, Kilpatrick N, Bankier A, Savarirayan R, Lamandé SR, Lench NJ, Crawford PJ.
    Oral Dis; 2002 Sep 01; 8(5):249-53. PubMed ID: 12363109
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  • 16. Identifying polymorphism in enamelin gene in amelogenesis imperfecta (AI).
    Gopinath VK, Yoong TP, Yean CY, Ravichandran M.
    Arch Oral Biol; 2008 Oct 01; 53(10):937-40. PubMed ID: 18466877
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  • 18. Amelogenin p.M1T and p.W4S mutations underlying hypoplastic X-linked amelogenesis imperfecta.
    Kim JW, Simmer JP, Hu YY, Lin BP, Boyd C, Wright JT, Yamada CJ, Rayes SK, Feigal RJ, Hu JC.
    J Dent Res; 2004 May 01; 83(5):378-83. PubMed ID: 15111628
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  • 19. Enamelin/ameloblastin gene polymorphisms in autosomal amelogenesis imperfecta among Syrian families.
    Dashash M, Bazrafshani MR, Poulton K, Jaber S, Naeem E, Blinkhorn AS.
    J Investig Clin Dent; 2011 Feb 01; 2(1):16-22. PubMed ID: 25427323
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