BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

123 related articles for article (PubMed ID: 2977283)

  • 1. Huntington disease: finding the gene and after.
    Menkes JH
    Pediatr Neurol; 1988; 4(2):73-8. PubMed ID: 2977283
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 50(4):565-71. PubMed ID: 2886227
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome.
    Gusella JF; Tanzi RE; Bader PI; Phelan MC; Stevenson R; Hayden MR; Hofman KJ; Faryniarz AG; Gibbons K
    Nature; 1985 Nov 7-13; 318(6041):75-8. PubMed ID: 2997623
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phenotypic variation in 2 Huntington's disease families with linkage to chromosome 4.
    Sax DS; Bird ED; Gusella JF; Myers RH
    Neurology; 1989 Oct; 39(10):1332-6. PubMed ID: 2529452
    [TBL] [Abstract][Full Text] [Related]  

  • 5. New insights into the clinical features, pathogenesis and molecular genetics of Huntington disease.
    Kremer B; Weber B; Hayden MR
    Brain Pathol; 1992 Oct; 2(4):321-35. PubMed ID: 1341966
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Genetic bases in Huntington disease].
    Benítez J
    Neurologia; 1999 Apr; 14(4):172-9. PubMed ID: 10363492
    [TBL] [Abstract][Full Text] [Related]  

  • 7. DNA and Huntington's chorea.
    Watt DC; Edwards J
    Psychol Med; 1984 Nov; 14(4):729-32. PubMed ID: 6242494
    [No Abstract]   [Full Text] [Related]  

  • 8. Linkage studies in autosomal dominant facioscapulohumeral muscular dystrophy.
    Padberg G; Eriksson AW; Volkers WS; Bernini L; Van Loghem E; Meera Khan P; Nijenhuis LE; Pronk JC; Schreuder GM
    J Neurol Sci; 1984 Sep; 65(3):261-8. PubMed ID: 6593433
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Huntington disease: clinical, genetic, and social aspects.
    Nance MA
    J Geriatr Psychiatry Neurol; 1998; 11(2):61-70. PubMed ID: 9877527
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Interpretation of linkage data for a Huntington-like disorder mapping to 4p15.3.
    Lesperance MM; Burmeister M
    Am J Hum Genet; 2000 Jul; 67(1):262-3. PubMed ID: 10848501
    [No Abstract]   [Full Text] [Related]  

  • 11. [Genetic epidemiology of Huntington chorea in Chile].
    Cruz-Coke R
    Rev Med Chil; 1987 May; 115(5):483-5. PubMed ID: 2966430
    [No Abstract]   [Full Text] [Related]  

  • 12. Allele frequencies and linkage disequilibrium of polymorphic DNA markers of the Huntington disease region in the German population.
    Thies U; Bockel B; Gerdes B; Schröder K
    Hum Genet; 1993 Dec; 92(6):593-7. PubMed ID: 7903271
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autosomal-dominant dentatorubropallidoluysian atrophy in the United Kingdom.
    Warner TT; Lennox GG; Janota I; Harding AE
    Mov Disord; 1994 May; 9(3):289-96. PubMed ID: 8041369
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Huntington disease locus is most likely within 325 kilobases of the chromosome 4p telomere.
    Doggett NA; Cheng JF; Smith CL; Cantor CR
    Proc Natl Acad Sci U S A; 1989 Dec; 86(24):10011-4. PubMed ID: 2557612
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation.
    Bućan M; Zimmer M; Whaley WL; Poustka A; Youngman S; Allitto BA; Ormondroyd E; Smith B; Pohl TM; MacDonald M
    Genomics; 1990 Jan; 6(1):1-15. PubMed ID: 2137426
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Childhood manifestation of autosomal dominant polycystic kidney disease: no evidence for genetic heterogeneity.
    Gal A; Wirth B; Kääriäinen H; Lucotte G; Landais P; Gillessen-Kaesbach G; Müller-Wiefel DE; Zerres K
    Clin Genet; 1989 Jan; 35(1):13-9. PubMed ID: 2924430
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Early onset Huntington disease: a neuronal degeneration syndrome.
    Seneca S; Fagnart D; Keymolen K; Lissens W; Hasaerts D; Debulpaep S; Desprechins B; Liebaers I; De Meirleir L
    Eur J Pediatr; 2004 Dec; 163(12):717-21. PubMed ID: 15338298
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Levodopa responsive parkinsonism in an adult with Huntington's disease.
    Racette BA; Perlmutter JS
    J Neurol Neurosurg Psychiatry; 1998 Oct; 65(4):577-9. PubMed ID: 9771791
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Huntington disease: genetics and epidemiology.
    Conneally PM
    Am J Hum Genet; 1984 May; 36(3):506-26. PubMed ID: 6233902
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Neurological disorders with autosomal dominant transmission.
    Simpson JM
    J Neurosurg Nurs; 1984 Oct; 16(5):262-9. PubMed ID: 6239015
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.