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:
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