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104 related items for PubMed ID: 1363458

  • 1. Friedreich's disease. A linkage study in southern and central Italy.
    Cavalcanti F, Cocozza S, Filla A, De Michele G, Pianese L, Porcellini A, Monticelli A, Pandolfo M, Banfi S, Varrone S.
    Acta Neurol (Napoli); 1992; 14(4-6):519-23. PubMed ID: 1363458
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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. The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15.
    Hanauer A, Chery M, Fujita R, Driesel AJ, Gilgenkrantz S, Mandel JL.
    Am J Hum Genet; 1990 Jan; 46(1):133-7. PubMed ID: 2294745
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  • 6. 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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  • 7. Mapping the Friedreich ataxia locus (FRDA) by linkage disequilibrium analysis with highly polymorphic microsatellites.
    Sirugo G, Duclos F, Fujita R, Keats JB, Pandolfo M, Mandel JL, Koenig M.
    Biomed Pharmacother; 1994 Dec; 48(5-6):219-24. PubMed ID: 7999982
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  • 8. Allele frequencies of DNA markers genetically linked to Friedreich ataxia in the German population.
    Zühlke C, Thies U.
    Hum Hered; 1993 Dec; 43(2):78-81. PubMed ID: 8103037
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  • 9. 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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  • 10. 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 Sep 06; 71(3):214-6. PubMed ID: 7587379
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  • 11. Physical mapping of two loci (D9S5 and D9S15) tightly linked to Friedreich ataxia locus (FRDA) and identification of nearby CpG islands by pulse-field gel electrophoresis.
    Fujita R, Hanauer A, Vincent A, Mandel JL, Koenig M.
    Genomics; 1991 Aug 06; 10(4):915-20. PubMed ID: 1916823
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  • 12. 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 06; 52(1):99-109. PubMed ID: 8434613
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  • 13. Prenatal diagnosis of Friedreich ataxia.
    Wallis J, Shaw J, Wilkes D, Farrall M, Williamson R, Chamberlain S, Skare JC, Milunsky A.
    Am J Med Genet; 1989 Nov 06; 34(3):458-61. PubMed ID: 2574535
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  • 16. Mapping of mutation causing Friedreich's ataxia to human chromosome 9.
    Chamberlain S, Shaw J, Rowland A, Wallis J, South S, Nakamura Y, von Gabain A, Farrall M, Williamson R.
    Nature; 1988 Jul 21; 334(6179):248-50. PubMed ID: 2899844
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  • 19. 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 21; 54(6):1050-9. PubMed ID: 8198128
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  • 20. Attempts to identify the chromosomal localization of the Friedreich's ataxia locus.
    Chamberlain S, Worrall C, Williamson R.
    Adv Neurol; 1988 Jun 21; 48():257-60. PubMed ID: 2891256
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