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Journal Abstract Search

160 related items for PubMed ID: 2903666

  • 1. Linkage studies in a large fragile X family.
    Patterson M, Bell M, Kress W, Davies KE, Froster-Iskenius U.
    Am J Hum Genet; 1988 Nov; 43(5):684-8. PubMed ID: 2903666
    [Abstract] [Full Text] [Related]

  • 2. Linkage between the fragile X and F9, DXS52 (St14), DXS98 (4D-8) and DXS105 (cX55.7).
    Mulley J, Turner G, Bain S, Sutherland GR.
    Am J Med Genet; 1988 Nov; 30(1-2):567-80. PubMed ID: 2902797
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  • 3. Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndrome.
    Thibodeau SN, Dorkins HR, Faulk KR, Berry R, Smith AC, Hagerman R, King A, Davies KE.
    Hum Genet; 1988 Jul; 79(3):219-27. PubMed ID: 3402993
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  • 4. Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families.
    Arveiler B, Oberlé I, Vincent A, Hofker MH, Pearson PL, Mandel JL.
    Am J Hum Genet; 1988 Feb; 42(2):380-9. PubMed ID: 2893549
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  • 5. Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304).
    Dahl N, Goonewardena P, Malmgren H, Gustavson KH, Holmgren G, Seemanova E, Annerén G, Flood A, Pettersson U.
    Am J Hum Genet; 1989 Aug; 45(2):304-9. PubMed ID: 2569270
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  • 6. DNA linkage analysis of 26 families with fragile X syndrome.
    Carpenter NJ.
    Am J Med Genet; 1991 Aug; 38(2-3):311-8. PubMed ID: 1673303
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  • 7. Linkage relationships between DXS105, DXS98, and other polymorphic DNA markers flanking the fragile X locus.
    Carpenter NJ, Thibodeau SN, Brown WT.
    Am J Med Genet; 1991 Aug; 38(2-3):349-53. PubMed ID: 1673310
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  • 12. The fragile X syndrome in a large family. III. Investigations on linkage of flanking DNA markers with the fragile site Xq27.
    Veenema H, Carpenter NJ, Bakker E, Hofker MH, Ward AM, Pearson PL.
    J Med Genet; 1987 Jul; 24(7):413-21. PubMed ID: 2886667
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  • 18. Fragile X syndrome: linkage analysis in black and white populations.
    Schwartz CE, Phelan MC, Brightharp C, Pancoast I, Howard-Peebles PN, Thibodeau S, Brown WT, Jenkins EC.
    Am J Med Genet; 1988 Jul; 30(1-2):531-42. PubMed ID: 3177470
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  • 19. Genetic and physical mapping of a novel region close to the fragile X site on the human X chromosome.
    Patterson MN, Bell MV, Bloomfield J, Flint T, Dorkins H, Thibodeau SN, Schaid D, Bren G, Schwartz CE, Wieringa B.
    Genomics; 1989 May; 4(4):570-8. PubMed ID: 2744766
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