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Journal Abstract Search

436 related items for PubMed ID: 2886667

  • 1. 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
    [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 Jul; 30(1-2):567-80. PubMed ID: 2902797
    [Abstract] [Full Text] [Related]

  • 3. The genetic distance between the coagulation factor IX gene and the locus for the fragile X syndrome: clinical implications.
    Forster-Gibson CJ, Mulligan LM, Partington MW, Simpson NE, Holden JJ, White BN.
    J Neurogenet; 1985 Jun; 2(3):231-7. PubMed ID: 3860635
    [Abstract] [Full Text] [Related]

  • 4. DNA linkage analysis of 26 families with fragile X syndrome.
    Carpenter NJ.
    Am J Med Genet; 1991 Jun; 38(2-3):311-8. PubMed ID: 1673303
    [Abstract] [Full Text] [Related]

  • 5. Genetic linkage heterogeneity in the fragile X syndrome.
    Brown WT, Gross AC, Chan CB, Jenkins EC.
    Hum Genet; 1985 Jun; 71(1):11-8. PubMed ID: 2993154
    [Abstract] [Full Text] [Related]

  • 6. DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity.
    Brown WT, Gross AC, Chan CB, Jenkins EC.
    Am J Med Genet; 1986 Jun; 23(1-2):643-64. PubMed ID: 3006490
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. 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 Apr; 23(1-2):665-83. PubMed ID: 3006491
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14.
    Mulley JC, Gedeon AK, Thorn KA, Bates LJ, Sutherland GR.
    Am J Med Genet; 1987 Jun; 27(2):435-48. PubMed ID: 2886048
    [Abstract] [Full Text] [Related]

  • 13. 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 Jun; 44():137-54. PubMed ID: 2895523
    [Abstract] [Full Text] [Related]

  • 14. Multipoint linkage of 9 anonymous probes to HPRT, factor 9, and fragile X.
    Brown WT, Ye W, Gross AC, Chan CB, Dobkin CS, Jenkins EC.
    Am J Med Genet; 1988 Jun; 30(1-2):551-66. PubMed ID: 2902796
    [Abstract] [Full Text] [Related]

  • 15. 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 Jun; 38(2-3):349-53. PubMed ID: 1673310
    [Abstract] [Full Text] [Related]

  • 16. Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardation.
    Voelckel MA, Mattei MG, N'Guyen C, Philip N, Birg F, Mattei JF.
    Hum Genet; 1988 Dec; 80(4):375-8. PubMed ID: 2904402
    [Abstract] [Full Text] [Related]

  • 17. Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation.
    Voelckel MA, Philip N, Piquet C, Pellissier MC, Oberlé I, Birg F, Mattei MG, Mattei JF.
    Hum Genet; 1989 Mar; 81(4):353-7. PubMed ID: 2564838
    [Abstract] [Full Text] [Related]

  • 18. 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
    [Abstract] [Full Text] [Related]

  • 19. The fragile X syndrome.
    Brown WT.
    Neurol Clin; 1989 Feb; 7(1):107-21. PubMed ID: 2646518
    [Abstract] [Full Text] [Related]

  • 20. Linkage in fragile X families of three distal flanking markers: ST14, DX13, and F8.
    Brown WT, Gross AC, Goonewardena P, Ferrando C, Dobkin C, Jenkins EC.
    Am J Med Genet; 1991 Feb; 38(2-3):343-6. PubMed ID: 1673308
    [Abstract] [Full Text] [Related]

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