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Journal Abstract Search

169 related items for PubMed ID: 1968042

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27-q28.
    Oostra BA, Majoor-Krakauer DF, van Hemel JO, Bakker E, Callen DF, Schmidt M, van Oost BA.
    Am J Med Genet; 1991 Jan; 38(2-3):332-5. PubMed ID: 1673306
    [Abstract] [Full Text] [Related]

  • 3. 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 Jan; 38(2-3):336-42. PubMed ID: 1673307
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridization.
    Schnur RE, Ledbetter SA, Ledbetter DH, Merry DE, Nussbaum RL.
    Am J Hum Genet; 1989 Feb; 44(2):248-54. PubMed ID: 2563194
    [Abstract] [Full Text] [Related]

  • 8. 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 Feb; 38(2-3):322-7. PubMed ID: 1673305
    [Abstract] [Full Text] [Related]

  • 9. Genetic mapping of new RFLPs at Xq27-q28.
    Suthers GK, Oberlé I, Nancarrow J, Mulley JC, Hyland VJ, Wilson PJ, McCure J, Morris CP, Hopwood JJ, Mandel JL.
    Genomics; 1991 Jan; 9(1):37-43. PubMed ID: 1672291
    [Abstract] [Full Text] [Related]

  • 10. Linkage analysis in the fragile X syndrome using multiple distal Xq polymorphic DNA markers.
    Glass IA, Pirrit LA, White EM, Bell MV, Davies KE, Cockburn F, Connor JM.
    Am J Med Genet; 1991 Jan; 38(2-3):298-304. PubMed ID: 1673301
    [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 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 May; 30(1-2):567-80. PubMed ID: 2902797
    [Abstract] [Full Text] [Related]

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  • 14. New distal marker closely linked to the fragile X locus.
    Hulsebos TJ, Oostra BA, Broersen S, Smits A, van Oost BA, Westerveld A.
    Hum Genet; 1991 Jul; 87(3):369-72. PubMed ID: 1677926
    [Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. 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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  • 19. 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]

  • 20. Genetic mapping of two new DNA markers in Xq26-q28 relative to the fragile-X syndrome locus.
    Sood R, Mulligan LM, Poon R, White BN, Holden JJ.
    Am J Hum Genet; 1990 Sep; 47(3):395-402. PubMed ID: 1975476
    [Abstract] [Full Text] [Related]

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