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Results: 5

Authors: Gaspar, C Lopes-Cendes, I Hayes, S Goto, J Arvidsson, K Dias, A Silveira, I Maciel, P Coutinho, P Lima, M Zhou, YX Soong, BW Watanabe, M Giunti, P Stevanin, G Riess, O Sasaki, H Hsieh, M Nicholson, GA Brunt, E Higgins, JJ Lauritzen, M Tranebjaerg, L Volpini, V Wood, N Ranum, L Tsuji, S Brice, A Sequeiros, J Rouleau, GA
Citation: C. Gaspar et al., Ancestral origins of the Machado-Joseph disease mutation: A worldwide haplotype study, AM J HU GEN, 68(2), 2001, pp. 523-528

Authors: Worth, PF Houlden, H Giunti, P Davis, MB Wood, NW
Citation: Pf. Worth et al., Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia, NAT GENET, 24(3), 2000, pp. 214-215

Authors: Stevanin, G David, G Durr, A Giunti, P Benomar, A Abada-Bendib, M Lee, MS Agid, Y Brice, A
Citation: G. Stevanin et al., Multiple origins of the spinocerebellar ataxia 7 (SCA7) mutation revealed by linkage disequilibrium studies with closely flanking markers, including an intragenic polymorphism (G(3145)TG/A(3145)TG), EUR J HUM G, 7(8), 1999, pp. 889-896

Authors: Worth, PF Giunti, P Gardner-Thorpe, C Dixon, PH Davis, MB Wood, NW
Citation: Pf. Worth et al., Autosomal dominant cerebellar ataxia type III: Linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3, AM J HU GEN, 65(2), 1999, pp. 420-426

Authors: Giunti, P Stevanin, G Worth, PF David, G Brice, A Wood, NW
Citation: P. Giunti et al., Molecular and clinical study of 18 families with ADCA type II: Evidence for genetic heterogeneity and De Novo mutation, AM J HU GEN, 64(6), 1999, pp. 1594-1603
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