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Journal Abstract Search

137 related items for PubMed ID: 1673304

  • 1. Carrier detection of the fragile X syndrome using flanking loci DXS98, DXS105, and DXS304.
    Dahl N, Malmgren H, Pettersson U, Holmgren G, Seemanová E, Gustavson KH.
    Am J Med Genet; 1991; 38(2-3):319-21. PubMed ID: 1673304
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  • 2. Linkage analysis of the fragile X syndrome using a new DNA marker U6.2 defining locus DXS304.
    Goonewardena P, Brown WT, Gross AC, Ferrando C, Dobkin C, Romano V, Bosco P, Ceratto N, Pettersson U, Dahl N.
    Am J Med Genet; 1991; 38(2-3):322-7. PubMed ID: 1673305
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  • 3. 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; 38(2-3):349-53. PubMed ID: 1673310
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  • 4. Carrier detection of the fragile X syndrome with flanking RFLP markers and linkage analysis.
    Väisänen ML, Kähkönen M, Leisti J.
    Am J Med Genet; 1991; 43(1-2):307-11. PubMed ID: 1351364
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  • 6. 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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  • 7. 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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  • 11. 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 Aug; 30(1-2):567-80. PubMed ID: 2902797
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  • 15. New informative polymorphism at the DXS304 locus, a close distal marker for the fragile X locus.
    Rousseau F, Vincent A, Oberlé I, Mandel JL.
    Hum Genet; 1990 Feb; 84(3):263-6. PubMed ID: 1968034
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  • 17. A new DNA probe of potential use for diagnosis of the fragile-X syndrome.
    Lucotte G.
    Ann Genet; 1990 Feb; 33(2):109-10. PubMed ID: 1978629
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  • 18. New polymorphism and a new chromosome breakpoint establish the physical and genetic mapping of DXS369 in the DXS98-FRAXA interval.
    Oberlé I, Vincent A, Abbadi N, Rousseau F, Hupkes PE, Hors-Cayla MC, Gilgenkrantz S, Oostra BA, Mandel JL.
    Am J Med Genet; 1991 Feb; 38(2-3):336-42. PubMed ID: 1673307
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  • 19. 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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