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Journal Abstract Search

142 related items for PubMed ID: 7485155

  • 21. Friedreich ataxia.
    Johnson WG.
    Clin Neurosci; 1995; 3(1):33-8. PubMed ID: 7614092
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  • 22. 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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  • 29. Trinucleotide (GAA)n repeat expansion in two families with Friedreich's ataxia with retained reflexes.
    Kellett MW, Fletcher NA, Wood N, Enevoldson TP.
    J Neurol Neurosurg Psychiatry; 1997 Dec; 63(6):780-3. PubMed ID: 9416816
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  • 31. Linkage disequilibrium and haplotype analysis in German Friedreich ataxia families.
    Zühlke C, Gehlken U, Purmann S, Kunisch M, Müller-Myhsok B, Kreuz F, Laccone F.
    Hum Hered; 1999 Mar; 49(2):90-6. PubMed ID: 10077729
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  • 32. Genotype and phenotype analysis of Friedreich's ataxia compound heterozygous patients.
    De Castro M, García-Planells J, Monrós E, Cañizares J, Vázquez-Manrique R, Vílchez JJ, Urtasun M, Lucas M, Navarro G, Izquierdo G, Moltó MD, Palau F.
    Hum Genet; 2000 Jan; 106(1):86-92. PubMed ID: 10982187
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  • 33. Early-onset ataxia with cardiomyopathy and retained tendon reflexes maps to the Friedreich's ataxia locus on chromosome 9q.
    Palau F, De Michele G, Vilchez JJ, Pandolfo M, Monrós E, Cocozza S, Smeyers P, Lopez-Arlandis J, Campanella G, Di Donato S.
    Ann Neurol; 1995 Mar; 37(3):359-62. PubMed ID: 7695235
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  • 36. Late onset Friedreich's disease: clinical features and mapping of mutation to the FRDA locus.
    De Michele G, Filla A, Cavalcanti F, Di Maio L, Pianese L, Castaldo I, Calabrese O, Monticelli A, Varrone S, Campanella G.
    J Neurol Neurosurg Psychiatry; 1994 Aug; 57(8):977-9. PubMed ID: 8057123
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  • 37. The canine FRDA gene maps to CFA 1q31.1-->q31.3.
    Kuiper H, Drögemüller C, Rak S, Leeb T, Quignon P, André C, Distl O.
    Cytogenet Genome Res; 2002 Aug; 98(4):311A. PubMed ID: 12826760
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  • 38. G130V, a common FRDA point mutation, appears to have arisen from a common founder.
    Delatycki MB, Knight M, Koenig M, Cossée M, Williamson R, Forrest SM.
    Hum Genet; 1999 Oct; 105(4):343-6. PubMed ID: 10543403
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  • 39. The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA gene.
    Forrest SM, Knight M, Delatycki MB, Paris D, Williamson R, King J, Yeung L, Nassif N, Nicholson GA.
    Neurogenetics; 1998 Aug; 1(4):253-7. PubMed ID: 10732799
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  • 40. 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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