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Journal Abstract Search

110 related items for PubMed ID: 2890502

  • 21. Two additional RFLPs at the D4S10 locus, useful for Huntington's disease (HD)-family studies.
    Bakker E, Skraastad MI, Fisser-Groen YM, van Ommen GJ, Pearson PL.
    Nucleic Acids Res; 1987 Nov 11; 15(21):9100. PubMed ID: 2891108
    [No Abstract] [Full Text] [Related]

  • 22. A somatic cell hybrid panel for localizing DNA segments near the Huntington's disease gene.
    MacDonald ME, Anderson MA, Gilliam TC, Tranejaerg L, Carpenter NJ, Magenis E, Hayden MR, Healey ST, Bonner TI, Gusella JF.
    Genomics; 1987 Sep 11; 1(1):29-34. PubMed ID: 2889660
    [Abstract] [Full Text] [Related]

  • 23. Genetic linkage between Huntington's disease and D4S10 (G8) in Scottish families.
    Holloway S, Millan FA, Curtis A, Mennie M, Brock DJ.
    Clin Genet; 1989 Feb 11; 35(2):133-8. PubMed ID: 2524298
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  • 24. A polymorphic DNA marker genetically linked to Huntington's disease.
    Gusella JF, Wexler NS, Conneally PM, Naylor SL, Anderson MA, Tanzi RE, Watkins PC, Ottina K, Wallace MR, Sakaguchi AY.
    Nature; 1989 Feb 11; 306(5940):234-8. PubMed ID: 6316146
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  • 25. Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales families.
    Harper PS, Youngman S, Anderson MA, Sarfarazi M, Quarrell O, Tanzi R, Shaw D, Wallace P, Conneally PM, Gusella JF.
    J Med Genet; 1985 Dec 11; 22(6):447-50. PubMed ID: 3001311
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  • 27. Studies on DNA markers (D4S10 and D4S43/S127) genetically linked to Huntington's disease in Japanese families.
    Kanazawa I, Kondo I, Ikeda JE, Ikeda T, Shizu Y, Yoshida M, Narabayashi H, Kuroda S, Tsunoda H, Mizuta E.
    Hum Genet; 1990 Aug 11; 85(3):257-60. PubMed ID: 1975553
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  • 28. Mapping of D4S98/S114/S113 confines the Huntington's defect to a reduced physical region at the telomere of chromosome 4.
    Whaley WL, Michiels F, MacDonald ME, Romano D, Zimmer M, Smith B, Leavitt J, Bucan M, Haines JL, Gilliam TC.
    Nucleic Acids Res; 1988 Dec 23; 16(24):11769-80. PubMed ID: 2905444
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  • 30. cDNA sequence and chromosomal localization of the mouse parvalbumin gene, Pva.
    Zühlke C, Schöffl F, Jockusch H, Simon D, Guénet JL.
    Genet Res; 1989 Aug 23; 54(1):37-43. PubMed ID: 2572511
    [Abstract] [Full Text] [Related]

  • 31. Non-random association between DNA markers and Huntington disease locus in the Italian population.
    Novelletto A, Mandich P, Bellone E, Malaspina P, Vivona G, Ajmar F, Frontali M.
    Am J Med Genet; 1991 Sep 01; 40(3):374-6. PubMed ID: 1683157
    [Abstract] [Full Text] [Related]

  • 32. Studies of a DNA marker (G8) genetically linked to Huntington disease in British families.
    Youngman S, Sarfarazi M, Quarrell OW, Conneally PM, Gibbons K, Harper PS, Shaw DJ, Tanzi RE, Wallace MR, Gusella JF.
    Hum Genet; 1986 Aug 01; 73(4):333-9. PubMed ID: 3017842
    [Abstract] [Full Text] [Related]

  • 33. Synteny on mouse chromosome 5 of homologs for human DNA loci linked to the Huntington disease gene.
    Cheng SV, Martin GR, Nadeau JH, Haines JL, Bucan M, Kozak CA, MacDonald ME, Lockyer JL, Ledley FD, Woo SL.
    Genomics; 1989 Apr 01; 4(3):419-26. PubMed ID: 2523855
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  • 34. Mapping of the mouse fibronectin gene (Fn-1) to chromosome 1: conservation of the Idh-1-Cryg-Fn-1 synteny group in mammals.
    Skow LC, Adkison L, Womack JE, Beamer WG, Taylor BA.
    Genomics; 1987 Nov 01; 1(3):283-6. PubMed ID: 2895729
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  • 36. The aryl hydrocarbon hydroxylase (Ah) locus and a novel restriction-fragment length polymorphism (RFLP) are located on mouse chromosome 12.
    Cobb RR, Stoming TA, Whitney JB.
    Biochem Genet; 1987 Jun 01; 25(5-6):401-13. PubMed ID: 2887160
    [Abstract] [Full Text] [Related]

  • 37. Recombination events suggest potential sites for the Huntington's disease gene.
    MacDonald ME, Haines JL, Zimmer M, Cheng SV, Youngman S, Whaley WL, Wexler N, Bucan M, Allitto BA, Smith B.
    Neuron; 1989 Aug 01; 3(2):183-90. PubMed ID: 2576211
    [Abstract] [Full Text] [Related]

  • 38. Considerations in using linkage analysis as a presymptomatic test for Huntington's disease.
    Farrer LA, Myers RH, Cupples LA, Conneally PM.
    J Med Genet; 1988 Sep 01; 25(9):577-88. PubMed ID: 2903248
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