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Journal Abstract Search

126 related items for PubMed ID: 7914465

  • 1. Linkage disequilibrium analysis of Friedreich's ataxia in 140 Caucasian families: positioning of the disease locus and evaluation of allelic heterogeneity.
    Sirugo G, Cocozza S, Brice A, Cavalcanti F, De Michele G, Dones I, Filla A, Koenig M, Lorenzetti D, Monticelli A.
    Eur J Hum Genet; 1993; 1(2):133-43. PubMed ID: 7914465
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  • 2. Additional polymorphisms at marker loci D9S5 and D9S15 generate extended haplotypes in linkage disequilibrium with Friedreich ataxia.
    Fujita R, Hanauer A, Sirugo G, Heilig R, Mandel JL.
    Proc Natl Acad Sci U S A; 1990 Mar; 87(5):1796-800. PubMed ID: 1968638
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  • 5. Recombinations in individuals homozygous by descent localize the Friedreich ataxia locus in a cloned 450-kb interval.
    Rodius F, Duclos F, Wrogemann K, Le Paslier D, Ougen P, Billault A, Belal S, Musenger C, Brice A, Dürr A.
    Am J Hum Genet; 1994 Jun; 54(6):1050-9. PubMed ID: 8198128
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  • 7. Identification of a hypervariable microsatellite polymorphism within D9S15 tightly linked to Friedrich's ataxia.
    Wallis J, Williamson R, Chamberlain S.
    Hum Genet; 1990 Jun; 85(1):98-100. PubMed ID: 2358306
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  • 9. Linkage disequilibrium between FD1-D9S202 haplotypes and the Friedreich's ataxia locus in a central-southern Italian population.
    Pianese L, Cocozza S, Campanella G, Castaldo I, Cavalcanti F, De Michele G, Filla A, Monticelli A, Munaro M, Redolfi E.
    J Med Genet; 1994 Feb; 31(2):133-5. PubMed ID: 8182719
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  • 10. Genetic recombination events which position the Friedreich ataxia locus proximal to the D9S15/D9S5 linkage group on chromosome 9q.
    Chamberlain S, Farrall M, Shaw J, Wilkes D, Carvajal J, Hillerman R, Doudney K, Harding AE, Williamson R, Sirugo G.
    Am J Hum Genet; 1993 Jan; 52(1):99-109. PubMed ID: 8434613
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  • 11. Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypes.
    Sirugo G, Keats B, Fujita R, Duclos F, Purohit K, Koenig M, Mandel JL.
    Am J Hum Genet; 1992 Mar; 50(3):559-66. PubMed ID: 1347194
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  • 12. A 530kb YAC contig tightly linked to the Friedreich ataxia locus contains five CpG clusters and a new highly polymorphic microsatellite.
    Fujita R, Sirugo G, Duclos F, Abderrahim H, Le Paslier D, Cohen D, Brownstein BH, Schlessinger D, Mandel JL, Koenig M.
    Hum Genet; 1992 Jul; 89(5):531-8. PubMed ID: 1353054
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  • 13. Physical evidence for the position of the Friedreich's ataxia locus FRDA proximal to D9S5.
    Hillermann R, See CG, Pook M, Wilkes D, Carvajal J, Doudney K, Williamson R, Chamberlain S.
    Cytogenet Cell Genet; 1995 Jul; 71(3):214-6. PubMed ID: 7587379
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  • 16. Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus.
    Belal S, Panayides K, Sirugo G, Ben Hamida C, Ioannou P, Hentati F, Beckmann J, Koenig M, Mandel JL, Ben Hamida M.
    Am J Hum Genet; 1992 Dec; 51(6):1372-6. PubMed ID: 1463017
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  • 19. Friedreich ataxia in Acadian families from eastern Canada: clinical diversity with conserved haplotypes.
    Richter A, Poirier J, Mercier J, Julien D, Morgan K, Roy M, Gosselin F, Bouchard JP, Melançon SB.
    Am J Med Genet; 1996 Sep 06; 64(4):594-601. PubMed ID: 8870928
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  • 20. Evidence of a genetic marker associated with early onset in Friedreich's ataxia.
    Cocozza S, Antonelli A, Campanella G, Cavalcanti F, De Michele G, Di Donato S, Filla A, Monticelli A, Pianese L, Piccinelli A.
    J Neurol; 1993 Sep 06; 240(4):254-6. PubMed ID: 8496716
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