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Dubourg, O
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Maisonobe, T
Brice, A
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Pingault, V
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Dubourg, O
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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
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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