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Results: 1-6 |
Results: 6

Authors: He, Y Jones, KJ Vignier, N Morgan, G Chevallay, M Barois, A Estournet-Mathiaud, B Hori, H Mizuta, T Tome, FMS North, KN Guicheney, P
Citation: Y. He et al., Congenital muscular dystrophy with primary partial laminin alpha 2 chain deficiency: Molecular study, NEUROLOGY, 57(7), 2001, pp. 1319-1322

Authors: Talim, B Ferreiro, A Cormand, B Vignier, N Oto, A Gogus, S Cila, A Lehesjoki, AE Pihko, H Guicheney, P Topaloglu, H
Citation: B. Talim et al., Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB loci, NEUROMUSC D, 10(8), 2000, pp. 548-552

Authors: Vilquin, JT Vignier, N Tremblay, JP Engvall, E Schwartz, K Fiszman, M
Citation: Jt. Vilquin et al., Identification of homozygous and heterozygous dy(2J) mice by PCR, NEUROMUSC D, 10(1), 2000, pp. 59-62

Authors: Di Blasi, C Mora, M Pareyson, D Farina, L Sghirlanzoni, A Vignier, N Blasevich, F Cornelio, F Guicheney, P Morandi, L
Citation: C. Di Blasi et al., Partial laminin alpha 2 chain deficiency in a patient with myopathy resembling inclusion body myositis, ANN NEUROL, 47(6), 2000, pp. 811-816

Authors: Neyroud, N Richard, P Vignier, N Donger, C Denjoy, I Demay, L Shkolnikova, M Pesce, R Chevalier, P Hainque, B Coumel, P Schwartz, K Guicheney, P
Citation: N. Neyroud et al., Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome, CIRCUL RES, 84(3), 1999, pp. 290-297

Authors: Vignier, N Moghadaszadeh, B Gary, F Beckmann, J Mayer, U Guicheney, P
Citation: N. Vignier et al., Structure, genetic localization, and identification of the cardiac and skeletal muscle transcripts of the human integrin alpha 7 gene (ITGA7), BIOC BIOP R, 260(2), 1999, pp. 357-364
Risultati: 1-6 |