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Journal Abstract Search

126 related items for PubMed ID: 1673301

  • 1. 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; 38(2-3):298-304. PubMed ID: 1673301
    [Abstract] [Full Text] [Related]

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

  • 3. 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]

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

  • 5. 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]

  • 6. Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions.
    Connor JM, Pirrit LA, Yates JR, Crossley JA, Imrie SJ, Colgan JM.
    J Med Genet; 1987 Jan; 24(1):14-22. PubMed ID: 2879932
    [Abstract] [Full Text] [Related]

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  • 8. 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 Jan; 38(2-3):343-6. PubMed ID: 1673308
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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 Aug; 38(2-3):332-5. PubMed ID: 1673306
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. 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]

  • 13. Carrier detection of the fragile X syndrome with flanking RFLP markers and linkage analysis.
    Väisänen ML, Kähkönen M, Leisti J.
    Am J Med Genet; 1990 Sep; 43(1-2):307-11. PubMed ID: 1351364
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. 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]

  • 16. 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]

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

  • 18. 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 Nov; 30(1-2):551-66. PubMed ID: 2902796
    [Abstract] [Full Text] [Related]

  • 19. Genetic and physical mapping of a novel region close to the fragile X site on the human X chromosome.
    Patterson MN, Bell MV, Bloomfield J, Flint T, Dorkins H, Thibodeau SN, Schaid D, Bren G, Schwartz CE, Wieringa B.
    Genomics; 1989 May; 4(4):570-8. PubMed ID: 2744766
    [Abstract] [Full Text] [Related]

  • 20. Carrier detection of the fragile X syndrome using flanking loci DXS98, DXS105, and DXS304.
    Dahl N, Malmgren H, Pettersson U, Holmgren G, Seemanová E, Gustavson KH.
    Am J Med Genet; 1991 May; 38(2-3):319-21. PubMed ID: 1673304
    [Abstract] [Full Text] [Related]

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