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

111 related items for PubMed ID: 2883080

  • 1. Effect of age-at-onset specifications on Huntington disease--G8 linkage analysis.
    Harris EL, Bale SJ.
    Genet Epidemiol Suppl; 1986; 1():229-33. PubMed ID: 2883080
    [No Abstract] [Full Text] [Related]

  • 2. Analysis of Huntington disease linkage to G8.
    Haines JL, Yount EA, Conneally PM.
    Genet Epidemiol Suppl; 1986; 1():223-8. PubMed ID: 2883079
    [No Abstract] [Full Text] [Related]

  • 3. Linkage analysis between Huntington disease and the G8 marker locus.
    Badner JA, Chakravarti A, Buetow KH.
    Genet Epidemiol Suppl; 1986; 1():211-6. PubMed ID: 2883077
    [No Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Analysis of Huntington disease linkage and age-of-onset distributions.
    Haynes C, Pericak-Vance M, Dawson D.
    Genet Epidemiol Suppl; 1986; 1():235-9. PubMed ID: 2883081
    [No Abstract] [Full Text] [Related]

  • 6. 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]

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

  • 8. 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]

  • 9. 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; 73(4):333-9. PubMed ID: 3017842
    [Abstract] [Full Text] [Related]

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

  • 11. Huntington disease: no evidence for locus heterogeneity.
    Conneally PM, Haines JL, Tanzi RE, Wexler NS, Penchaszadeh GK, Harper PS, Folstein SE, Cassiman JJ, Myers RH, Young AB.
    Genomics; 1989 Aug; 5(2):304-8. PubMed ID: 2571579
    [Abstract] [Full Text] [Related]

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

  • 13. 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; 22(6):447-50. PubMed ID: 3001311
    [Abstract] [Full Text] [Related]

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

  • 15. 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]

  • 16. 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]

  • 17. Genetic analysis workshop IV: Huntington disease linkage analysis summary.
    Pericak-Vance MA, Meyers DA.
    Genet Epidemiol Suppl; 1986 Jan; 1():197-209. PubMed ID: 2952549
    [No Abstract] [Full Text] [Related]

  • 18. An anonymous genomic clone that detects a frequent RFLP adjacent to the D4S10 (G8) marker and Huntington's disease.
    Carlock LR, Vo TD, DeHaven CR, Murray JC.
    Nucleic Acids Res; 1987 Jan 12; 15(1):377. PubMed ID: 2881254
    [No Abstract] [Full Text] [Related]

  • 19. DNA probes for presymptomatic diagnosis: keys to biological determinism?
    Harrison LC.
    Med J Aust; 1988 Jun 06; 148(11):546-7. PubMed ID: 2897619
    [No Abstract] [Full Text] [Related]

  • 20. Sequence analysis of three polymorphic regions in the human genome detected by the G8 probe for RFLPs associated with Huntington's disease.
    Stapleton PM.
    Nucleic Acids Res; 1988 Mar 25; 16(6):2735. PubMed ID: 2896333
    [No Abstract] [Full Text] [Related]

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