These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

120 related items for PubMed ID: 2883078

  • 1. Strategies for efficient linkage analysis: example of Huntington's disease pedigrees.
    Bishop DT, Cannon LA, Quigley AC, Skolnick MH.
    Genet Epidemiol Suppl; 1986; 1():217-22. PubMed ID: 2883078
    [No Abstract] [Full Text] [Related]

  • 2. Linkage analysis of G8 and Huntington's disease.
    Marazita ML, Spence MA.
    Genet Epidemiol Suppl; 1986; 1():247-50. PubMed ID: 2883083
    [No Abstract] [Full Text] [Related]

  • 3. Report on genetic linkage analysis between Huntington's disease and the G8 DNA polymorphism.
    Sarfarazi M.
    Genet Epidemiol Suppl; 1986; 1():259-64. PubMed ID: 2883084
    [No Abstract] [Full Text] [Related]

  • 4. Presymptomatic testing for Huntington's disease. A case complicated by recombination within the D4S10 locus.
    Curtis A, Millan F, Holloway S, Mennie M, Crosbie A, Raeburn JA, Brock DJ.
    Hum Genet; 1989 Jan; 81(2):188-90. PubMed ID: 2563253
    [Abstract] [Full Text] [Related]

  • 5. Absence of close linkage between benign hereditary chorea and the locus D4S10 (probe G8).
    Quarrell OW, Youngman S, Sarfarazi M, Harper PS.
    J Med Genet; 1988 Mar; 25(3):191-4. PubMed ID: 2895189
    [Abstract] [Full Text] [Related]

  • 6. 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; 3(2):183-90. PubMed ID: 2576211
    [Abstract] [Full Text] [Related]

  • 7. Linkage studies and prediction of risks for Huntington disease.
    Maestri NE, Beaty TH, Meyers DA.
    Genet Epidemiol Suppl; 1986 Aug; 1():241-6. PubMed ID: 2883082
    [No Abstract] [Full Text] [Related]

  • 8. A new DNA marker (D4S90) is located terminally on the short arm of chromosome 4, close to the Huntington disease gene.
    Youngman S, Sarfarazi M, Bucan M, MacDonald M, Smith B, Zimmer M, Gilliam C, Frischauf AM, Wasmuth JJ, Gusella JF.
    Genomics; 1989 Nov; 5(4):802-9. PubMed ID: 2574148
    [Abstract] [Full Text] [Related]

  • 9. Genetic linkage analysis and presymptomatic testing in Huntington's disease. First report in Italy.
    Di Maio L, Boiano S, Squitieri F, Napolitano G, Cocozza S, Campanella G, Battistuzzi G.
    Acta Neurol (Napoli); 1992 Nov; 14(4-6):524-9. PubMed ID: 1363459
    [Abstract] [Full Text] [Related]

  • 10. Huntington's disease: predictive testing and the molecular genetics laboratory.
    Lazarou LP, Meredith AL, Myring JM, Tyler A, Morris M, Ball DM, Harper PS.
    Clin Genet; 1993 Mar; 43(3):150-6. PubMed ID: 8098998
    [Abstract] [Full Text] [Related]

  • 11. Localization of the Huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomere.
    Gilliam TC, Tanzi RE, Haines JL, Bonner TI, Faryniarz AG, Hobbs WJ, MacDonald ME, Cheng SV, Folstein SE, Conneally PM.
    Cell; 1987 Aug 14; 50(4):565-71. PubMed ID: 2886227
    [Abstract] [Full Text] [Related]

  • 12. Molecular genetic strategies to investigate Huntington's disease.
    Gilliam TC, Gusella JF, Lehrach H.
    Adv Neurol; 1988 Aug 14; 48():17-29. PubMed ID: 2891255
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. 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 14; 35(2):133-8. PubMed ID: 2524298
    [Abstract] [Full Text] [Related]

  • 15. 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 14; 25(9):577-88. PubMed ID: 2903248
    [Abstract] [Full Text] [Related]

  • 16. [DNA markers linked to Huntington's disease (D4S10 and D4S95) in Spanish families: preliminary results].
    Benítez J, Ramos C, Fernández E, Ayuso C, Yébenes J.
    Rev Clin Esp; 1992 Apr 14; 190(6):299-301. PubMed ID: 1350862
    [Abstract] [Full Text] [Related]

  • 17. Exclusion mapping of the hereditary dentatorubropallidoluysian atrophy gene from the Huntington's disease locus.
    Kondo I, Ohta H, Yazaki M, Ikeda JE, Gusella JF, Kanazawa I.
    J Med Genet; 1990 Feb 14; 27(2):105-8. PubMed ID: 1969487
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. 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 14; 22(6):447-50. PubMed ID: 3001311
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.