AAAAAA

   
Results: 1-6 |
Results: 6

Authors: Balzergue, S Dubreucq, B Chauvin, S Le-Clainche, I Le Boulaire, F de Rose, R Samson, F Biaudet, V Lecharny, A Cruaud, C Weissenbach, J Caboche, M Lepiniec, L
Citation: S. Balzergue et al., Improved PCR-walking for large-scale isolation of plant T-DNA borders, BIOTECHNIQU, 30(3), 2001, pp. 496

Authors: Nicole, S Davoine, CS Topaloglu, H Cattolico, L Barral, D Beighton, P Ben Hamida, C Hammouda, H Cruaud, C White, PS Samson, D Urtizberea, JA Lehmann-Horn, F Weissenbach, J Hentati, F Fontaine, B
Citation: S. Nicole et al., Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia), NAT GENET, 26(4), 2000, pp. 480-483

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: Bentolila, S Bach, JM Kessler, JL Bordelais, I Cruaud, C Weissenbach, J Panthier, JJ
Citation: S. Bentolila et al., Analysis of major repetitive DNA sequences in the dog (Canis familiaris) genome, MAMM GENOME, 10(7), 1999, pp. 699-705

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
Risultati: 1-6 |