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Journal Abstract Search

164 related items for PubMed ID: 3860635

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  • 2. DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity.
    Brown WT, Gross AC, Chan CB, Jenkins EC.
    Am J Med Genet; 1986; 23(1-2):643-64. PubMed ID: 3006490
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  • 8. Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.
    Mulligan LM, Phillips MA, Forster-Gibson CJ, Beckett J, Partington MW, Simpson NE, Holden JJ, White BN.
    Am J Hum Genet; 1985 May; 37(3):463-72. PubMed ID: 2988332
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  • 9. Linkage and recombination between fragile X-linked mental retardation and the factor IX gene.
    Warren ST, Glover TW, Davidson RL, Jagadeeswaran P.
    Hum Genet; 1985 May; 69(1):44-6. PubMed ID: 3967889
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  • 10. Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.
    Oberlé I, Heilig R, Moisan JP, Kloepfer C, Mattéi GM, Mattéi JF, Boué J, Froster-Iskenius U, Jacobs PA, Lathrop GM.
    Proc Natl Acad Sci U S A; 1986 Feb; 83(4):1016-20. PubMed ID: 3006023
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  • 11. Further evidence for genetic heterogeneity in the fragile X syndrome.
    Brown WT, Jenkins EC, Gross AC, Chan CB, Krawczun MS, Duncan CJ, Sklower SL, Fisch GS.
    Hum Genet; 1987 Apr; 75(4):311-21. PubMed ID: 2883105
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  • 12. 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 Apr; 30(1-2):567-80. PubMed ID: 2902797
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  • 13. [Recombination between the fragile site Xq27 and the gene for coagulation factor IX].
    Landoulsi A, de Blois MC, Guérin P, Rethoré MO, Lejeune J, Lucotte G.
    Ann Genet; 1985 Apr; 28(4):201-5. PubMed ID: 3879429
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  • 14. The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locus.
    Vincent A, Dahl N, Oberlé I, Hanauer A, Mandel JL, Malmgren H, Pettersson U.
    Genomics; 1989 Nov; 5(4):797-801. PubMed ID: 2574147
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  • 15. 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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  • 16. New polymorphic DNA marker close to the fragile site FRAXA.
    Oostra BA, Hupkes PE, Perdon LF, van Bennekom CA, Bakker E, Halley DJ, Schmidt M, Du Sart D, Smits A, Wieringa B.
    Genomics; 1990 Jan; 6(1):129-32. PubMed ID: 1968042
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  • 17. 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 Jan; 38(2-3):349-53. PubMed ID: 1673310
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  • 18. The fragile X syndrome.
    Brown WT.
    Neurol Clin; 1989 Feb; 7(1):107-21. PubMed ID: 2646518
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