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Journal Abstract Search

76 related items for PubMed ID: 2776486

  • 1. Physical mapping of probes proximal to the fragile X locus (FRAX) confirms the order F9-DXS105 (cX55.7)-DXS98 (4D8)-FRAXA.
    Sauer SM, Phelan MC, Richer CL, Schwartz CE.
    Cytogenet Cell Genet; 1989; 50(2-3):172-3. PubMed ID: 2776486
    [Abstract] [Full Text] [Related]

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

  • 4. 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; 30(1-2):567-80. PubMed ID: 2902797
    [Abstract] [Full Text] [Related]

  • 5. Physical mapping studies on the human X chromosome in the region Xq27-Xqter.
    Patterson M, Schwartz C, Bell M, Sauer S, Hofker M, Trask B, van den Engh G, Davies KE.
    Genomics; 1987 Dec; 1(4):297-306. PubMed ID: 3482420
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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]

  • 8. 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]

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

  • 10. 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]

  • 11. 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]

  • 12. 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]

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

  • 14. Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is present.
    Schwartz C, Fitch N, Phelan MC, Richer CL, Stevenson R.
    Hum Genet; 1987 May; 76(1):54-7. PubMed ID: 3471705
    [Abstract] [Full Text] [Related]

  • 15. Physical mapping of the factor VIII gene proximal to two polymorphic DNA probes in human chromosome band Xq28: implications for factor VIII gene segregation analysis.
    Tantravahi U, Murty VV, Jhanwar SC, Toole JJ, Woozney JM, Chaganti RS, Latt SA.
    Cytogenet Cell Genet; 1986 May; 42(1-2):75-9. PubMed ID: 3013509
    [Abstract] [Full Text] [Related]

  • 16. Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation.
    Hofker MH, Bergen AA, Skraastad MI, Carpenter NJ, Veenema H, Connor JM, Bakker E, van Ommen GJ, Pearson PL.
    Am J Hum Genet; 1987 Apr; 40(4):312-28. PubMed ID: 2883888
    [Abstract] [Full Text] [Related]

  • 17. 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 Apr; 38(2-3):298-304. PubMed ID: 1673301
    [Abstract] [Full Text] [Related]

  • 18. Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site.
    Mattei MG, Baeteman MA, Heilig R, Oberlé I, Davies K, Mandel JL, Mattei JF.
    Hum Genet; 1985 Apr; 69(4):327-31. PubMed ID: 2985491
    [Abstract] [Full Text] [Related]

  • 19. Pulsed-field gel mapping studies in the vicinity of the fragile site at Xq27.3.
    Patterson M, Bell M, Schwartz C, Davies K.
    Am J Med Genet; 1988 Apr; 30(1-2):581-91. PubMed ID: 3177471
    [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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