AAAAAA

   
Results: 1-5 |
Results: 5

Authors: Bruls, T Gyapay, G Petit, JL Artiguenave, F Vico, V Qin, SZ Tin-Wollam, AM Da Silva, C Muselet, D Mavel, D Pelletier, E Levy, M Fujiyama, A Matsuda, F Wilson, R Rowen, L Hood, L Weissenbach, J Saurin, W Heilig, R
Citation: T. Bruls et al., A physical map of human chromosome 14, NATURE, 409(6822), 2001, pp. 947-948

Authors: Fonknechten, N Mavel, D Byrne, P Davoine, CS Cruaud, C Boentsch, D Samson, D Coutinho, P Hutchinson, M McMonagle, P Burgunder, JM Tartaglione, A Heinzlef, O Feki, I Deufel, T Parfrey, N Brice, A Fontaine, B Prud'homme, JF Weissenbach, J Durr, A Hazan, J
Citation: N. Fonknechten et al., Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia, HUM MOL GEN, 9(4), 2000, pp. 637-644

Authors: Hazan, J Fonknechten, N Mavel, D Paternotte, C Samson, D Artiguenave, F Davoine, CS Cruaud, C Durr, A Wincker, P Brottier, P Cattolico, L Barbe, V Burgunder, JM Prud'homme, JF Brice, A Fontaine, B Heilig, R Weissenbach, J
Citation: J. Hazan et al., Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia, NAT GENET, 23(3), 1999, pp. 296-303

Authors: Hazan, J Davoine, CS Mavel, D Fonknechten, N Paternotte, C Fizames, C Cruaud, C Samson, D Muselet, D Vega-Czarny, N Brice, A Gyapay, G Heilig, R Fontaine, B Weissenbach, J
Citation: J. Hazan et al., A fine integrated map of the SPG4 locus excludes an expanded CAG repeat inchromosome 2p-linked autosomal dominant spastic paraplegia, GENOMICS, 60(3), 1999, pp. 309-319

Authors: Paternotte, C Rudnicki, D Fizames, C Davoine, CS Mavel, D Durr, A Samson, D Marquette, C Muselet, D Vega-Czarny, N Drouot, N Voit, T Fontaine, B Gyapay, G Auburger, G Weissenbach, J Hazan, J
Citation: C. Paternotte et al., Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q, GENOME RES, 8(11), 1998, pp. 1216-1227
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