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Journal Abstract Search

444 related items for PubMed ID: 3502701

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

  • 2. 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]

  • 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 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]

  • 5. 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]

  • 6. Multilocus analysis of the fragile X syndrome.
    Brown WT, Gross A, Chan C, Jenkins EC, Mandel JL, Oberlé I, Arveiler B, Novelli G, Thibodeau S, Hagerman R.
    Hum Genet; 1988 Mar; 78(3):201-5. PubMed ID: 3162224
    [Abstract] [Full Text] [Related]

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

  • 8. 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]

  • 9. 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]

  • 10. The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locus.
    Vincent A, Dahl N, Oberlé I, Hanauer A, Mandel JL, Malmgren H, Pettersson U.
    Genomics; 1989 Nov; 5(4):797-801. PubMed ID: 2574147
    [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. 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 Jun; 30(1-2):567-80. PubMed ID: 2902797
    [Abstract] [Full Text] [Related]

  • 14. Infantile autism, fragile (X) (q27.3) and RFLP analysis in an extended Swedish family.
    Anvret M, Gillberg C, Wahlström J, Albertsson-Wikland K, Davies K.
    Clin Genet; 1988 Oct; 34(4):265-71. PubMed ID: 2906823
    [Abstract] [Full Text] [Related]

  • 15. 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
    [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. Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal Xq.
    Buchanan JA, Buckton KE, Gosden CM, Newton MS, Clayton JF, Christie S, Hastie N.
    Hum Genet; 1987 Jun; 76(2):165-72. PubMed ID: 3038730
    [Abstract] [Full Text] [Related]

  • 18. 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]

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  • 20. DNA studies of X-linked mental retardation associated with a fragile site at Xq27.3.
    Goonewardena P, Dahl N, Gustavson KH, Holmgren G, Pettersson U.
    Ups J Med Sci Suppl; 1987 Jan; 44():155-64. PubMed ID: 2895524
    [Abstract] [Full Text] [Related]

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