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Journal Abstract Search

211 related items for PubMed ID: 3674751

  • 1. Genetic heterogeneity of X-linked mental retardation with fragile X. Association of tight linkage to factor IX and incomplete penetrance in males.
    Giannelli F, Morris AH, Garrett C, Daker M, Thurston C, Smith CA.
    Ann Hum Genet; 1987 May; 51(2):107-24. PubMed ID: 3674751
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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 May; 23(1-2):643-64. PubMed ID: 3006490
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  • 3. Genetic linkage heterogeneity in the fragile X syndrome.
    Brown WT, Gross AC, Chan CB, Jenkins EC.
    Hum Genet; 1985 May; 71(1):11-8. PubMed ID: 2993154
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  • 5. 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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  • 9. Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome).
    Davies KE, Mattei MG, Mattei JF, Veenema H, McGlade S, Harper K, Tommerup N, Nielsen KB, Mikkelsen M, Beighton P.
    Hum Genet; 1985 Feb; 70(3):249-55. PubMed ID: 2991115
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  • 10. 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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  • 11. Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27.
    Oberlé I, Camerino G, Wrogemann K, Arveiler B, Hanauer A, Raimondi E, Mandel JL.
    Hum Genet; 1987 Sep; 77(1):60-5. PubMed ID: 3502701
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  • 13. Linkage heterogeneity and fragile X.
    Clayton JF, Gosden CM, Hastie ND, Evans HJ.
    Hum Genet; 1988 Apr; 78(4):338-42. PubMed ID: 2896154
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  • 14. 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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  • 15. 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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  • 16. [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 Aug; 28(4):201-5. PubMed ID: 3879429
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  • 17. Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male.
    Camerino G, Mattei MG, Mattei JF, Jaye M, Mandel JL.
    Nature; 1985 Aug; 306(5944):701-4. PubMed ID: 6689201
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  • 18. 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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  • 19. Genetics and expression of the fragile X syndrome.
    Brown WT, Jenkins EC, Gross AC, Chan CB, Wisniewski K, Cohen IL, Miezejeski CM.
    Ups J Med Sci Suppl; 1987 Jul; 44():137-54. PubMed ID: 2895523
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  • 20. An assessment of the use of flanking DNA markers for fra(X) syndrome carrier detection and prenatal diagnosis.
    Forster-Gibson CJ, Mulligan LM, Simpson NE, White BN, Holden JJ.
    Am J Med Genet; 1986 Jul; 23(1-2):665-83. PubMed ID: 3006491
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