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PUBMED FOR HANDHELDS

Journal Abstract Search

124 related items for PubMed ID: 12363109

  • 1.
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  • 2. An amelogenin gene defect associated with human X-linked amelogenesis imperfecta.
    Collier PM, Sauk JJ, Rosenbloom SJ, Yuan ZA, Gibson CW.
    Arch Oral Biol; 1997 Mar; 42(3):235-42. PubMed ID: 9188994
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  • 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. 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
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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. Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1).
    Lench NJ, Winter GB.
    Hum Mutat; 1995 Dec; 5(3):251-9. PubMed ID: 7599636
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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; 10(4):971-5. PubMed ID: 1916828
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  • 8. 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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  • 10. 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 01; 39(4):275-85. PubMed ID: 10218009
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  • 13. 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 01; 17(1):89-92. PubMed ID: 8406474
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  • 15. Molecular biology of hereditary enamel defects.
    Aldred MJ, Crawford PJ.
    Ciba Found Symp; 1997 Jul 01; 205():200-5; discussion 205-9. PubMed ID: 9189626
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  • 19. Understanding enamel formation from mutations causing X-linked amelogenesis imperfecta.
    Lagerström-Fermér M, Landegren U.
    Connect Tissue Res; 1995 Jul 01; 32(1-4):241-6. PubMed ID: 7554922
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