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Journal Abstract Search

238 related items for PubMed ID: 2988332

  • 1. 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]

  • 2. 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]

  • 3. 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]

  • 4. 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]

  • 5. 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]

  • 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. 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]

  • 8. 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]

  • 9. 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]

  • 10. 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]

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

  • 12. 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]

  • 13. 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]

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

  • 15. Cytogenetic and physical mapping in the region of the X chromosome surrounding the fragile site.
    Nguyen C, Mattei MG, Rey JA, Baeteman MA, Mattei JF, Jordan BR.
    Am J Med Genet; 1988 Sep; 30(1-2):601-11. PubMed ID: 2902799
    [Abstract] [Full Text] [Related]

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

  • 17. Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome).
    Davies KE, Mattei MG, Mattei JF, Veenema H, McGlade S, Harper K, Tommerup N, Nielsen KB, Mikkelsen M, Beighton P.
    Hum Genet; 1985 Sep; 70(3):249-55. PubMed ID: 2991115
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. In situ hybridization studies using a molecular probe that maps to Xq27-Zq28.
    Duncan AM, Morgan C.
    Hum Genet; 1990 Apr; 84(5):446-8. PubMed ID: 2323777
    [Abstract] [Full Text] [Related]

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

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