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Journal Abstract Search

182 related items for PubMed ID: 2063871

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  • 2. The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus.
    Kwiatkowski TJ, Orr HT, Banfi S, McCall AE, Jodice C, Persichetti F, Novelletto A, LeBorgne-DeMarquoy F, Duvick LA, Frontali M.
    Am J Hum Genet; 1993 Aug; 53(2):391-400. PubMed ID: 8101039
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  • 3. Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p.
    Ranum LP, Duvick LA, Rich SS, Schut LJ, Litt M, Orr HT.
    Am J Hum Genet; 1991 Jul; 49(1):31-41. PubMed ID: 1676561
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  • 7. Tight linkage of the gene for spinocerebellar ataxia to D6S89 on the short arm of chromosome 6 in a kindred for which close linkage to both HLA and F13A1 is excluded.
    Keats BJ, Pollack MS, McCall A, Wilensky MA, Ward LJ, Lu M, Zoghbi HY.
    Am J Hum Genet; 1991 Nov; 49(5):972-7. PubMed ID: 1928103
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  • 9. Spinocerebellar ataxia: multipoint linkage analysis of genes associated with the disease locus.
    Wilkie PJ, Schut LJ, Rich SS.
    Hum Genet; 1991 Aug; 87(4):405-8. PubMed ID: 1879827
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  • 13. Adult onset spinocerebellar ataxia linked to HLA in a South African kindred of mixed ancestry.
    Bryer A, Martell RW, du Toit ED, Beighton P.
    Tissue Antigens; 1992 Sep; 40(3):111-5. PubMed ID: 1440565
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  • 14. Mapping and cloning of the critical region for the spinocerebellar ataxia type 1 gene (SCA1) in a yeast artificial chromosome contig spanning 1.2 Mb.
    Banfi S, Chung MY, Kwiatkowski TJ, Ranum LP, McCall AE, Chinault AC, Orr HT, Zoghbi HY.
    Genomics; 1993 Dec; 18(3):627-35. PubMed ID: 8307572
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  • 15. Multipoint linkage analysis of spinocerebellar ataxia and markers on chromosome 6.
    Haines JL, Trofatter JA.
    Genet Epidemiol; 1986 Dec; 3(6):399-405. PubMed ID: 3468044
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  • 18. Localization of the hemochromatosis gene close to D6S105.
    Jazwinska EC, Lee SC, Webb SI, Halliday JW, Powell LW.
    Am J Hum Genet; 1993 Aug; 53(2):347-52. PubMed ID: 8328453
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  • 20. Expanded CAG repeats in spinocerebellar ataxia (SCA1) segregate with distinct haplotypes in South african families.
    Ramesar RS, Bardien S, Beighton P, Bryer A.
    Hum Genet; 1997 Jul; 100(1):131-7. PubMed ID: 9225982
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