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Journal Abstract Search

176 related items for PubMed ID: 1676561

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  • 9. 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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  • 10. Molecular heterogeneity of autosomal dominant cerebellar ataxia: analysis of flanking microsatellites of the spinocerebellar ataxia 1 locus in a northern European family unequivocally demonstrates non-linkage.
    Lunkes A, Gispert S, Enczmann J, Auburger G.
    Hum Genet; 1993 May; 91(4):362-6. PubMed ID: 8099059
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  • 11. Spinocerebellar ataxia (SCA1) in two large Italian kindreds: evidence in favour of a locus position distal to GLO1 and the HLA cluster.
    Frontali M, Iodice C, Lulli P, Spadaro M, Cappellacci S, Giunti P, Malaspina P, Morellini M, Morocutti C, Novelletto A.
    Ann Hum Genet; 1991 Jan; 55(1):7-15. PubMed ID: 1675045
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  • 12. Autosomal dominant spinocerebellar ataxia (SCA) in a Siberian founder population: assignment to the SCA1 locus.
    Lunkes A, Goldfarb LG, Platonov FA, Alexeev VP, Duenas-Barajas E, Gajdusek DC, Auburger G.
    Exp Neurol; 1994 Apr; 126(2):310-2. PubMed ID: 7925830
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  • 13. 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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  • 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. Presymptomatic analysis of spinocerebellar ataxia type 1 (SCA1) via the expansion of the SCA1 CAG-repeat in a large pedigree displaying anticipation and parental male bias.
    Matilla T, Volpini V, Genís D, Rosell J, Corral J, Dávalos A, Molins A, Estivill X.
    Hum Mol Genet; 1993 Dec; 2(12):2123-8. PubMed ID: 8111382
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  • 17. 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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  • 19. Spinocerebellar ataxia: localization of an autosomal dominant locus between two markers on human chromosome 6.
    Rich SS, Wilkie P, Schut L, Vance G, Orr HT.
    Am J Hum Genet; 1987 Oct; 41(4):524-31. PubMed ID: 3477955
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  • 20. HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindreds.
    Spadaro M, Giunti P, Lulli P, Frontali M, Jodice C, Cappellacci S, Morellini M, Persichetti F, Trabace S, Anastasi R.
    Acta Neurol Scand; 1992 Apr; 85(4):257-65. PubMed ID: 1585797
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