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Results: 1-6 |
Results: 6

Authors: Dubourg, O Tardieu, S Birouk, N Gouider, R Leger, JM Maisonobe, T Brice, A Bouche, P LeGuern, E
Citation: O. Dubourg et al., The frequency of 17p11.2 duplication and Connexin 32 mutations in 282 Charcot-Marie-Tooth families in relation to the mode of inheritance and motor nerve conduction velocity, NEUROMUSC D, 11(5), 2001, pp. 458-463

Authors: Pingault, V Bondurand, N Le Caignec, C Tardieu, S Lemort, N Dubourg, O Le Guern, E Goossens, M Boespflug-Tanguy, O
Citation: V. Pingault et al., The SOX10 transcription factor: evaluation as a candidate gene for centraland peripheral hereditary myelin disorders, J NEUROL, 248(6), 2001, pp. 496-499

Authors: Dubourg, O Tardieu, S Birouk, N Gouider, R Leger, JM Maisonobe, T Brice, A Bouche, P LeGuern, E
Citation: O. Dubourg et al., Clinical, electrophysiological and molecular genetic characteristics of 93patients with X-linked Charcot-Marie-Tooth disease, BRAIN, 124, 2001, pp. 1958-1967

Authors: Bernard, R Labelle, V Negre, P Tardieu, S Azulay, JP Malzac, P Mattei, JF Leguern, E Philip, N Levy, N
Citation: R. Bernard et al., Prenatal detection of a 17p11.2 duplication resulting from a rare recombination event and novel PCR-based strategy for molecular identification of Charcot-Marie-Tooth disease type 1A, EUR J HUM G, 8(3), 2000, pp. 229-235

Authors: Lopes, J Tardieu, S Silander, K Blair, I Vandenberghe, A Palau, F Ruberg, M Brice, A LeGuern, E
Citation: J. Lopes et al., Homologous DNA exchanges in humans can be explained by the yeast double-strand break repair model: a study of 17p11.2 rearrangements associated with CMT1A and HNPP, HUM MOL GEN, 8(12), 1999, pp. 2285-2292

Authors: Mouton, P Tardieu, S Gouider, R Birouk, N Maisonabe, T Dubourg, O Brice, A LeGuern, E Bouche, P
Citation: P. Mouton et al., Spectrum of clinical and electrophysiologic features in HNPP patients withthe 17p11.2 deletion, NEUROLOGY, 52(7), 1999, pp. 1440-1446
Risultati: 1-6 |