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Results: 4

Authors: Hamel, CP Griffoin, JM Bazalgette, C Lasquellec, L Duval, PA Bareil, C Beaufrere, L Bonnet, S Eliaou, C Marlhens, F Schmitt-Bernard, CF Tuffery, S Claustres, M Arnaud, B
Citation: Cp. Hamel et al., Molecular genetics of pigmentary retinopathies: Identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes, J FR OPHTAL, 23(10), 2000, pp. 985-995

Authors: Delague, V Bareil, C Tuffery, S Bouvagnet, P Chouery, E Koussa, S Maisonobe, T Loiselet, J Megarbane, A Claustres, M
Citation: V. Delague et al., Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: Exclusion of MAG as a candidate gene, AM J HU GEN, 67(1), 2000, pp. 236-243

Authors: Girardet, A Lien, S Leeflang, EP Beaufrere, L Tuffery, S Munier, F Arnheim, N Claustres, M Pellestor, F
Citation: A. Girardet et al., Direct estimation of the recombination frequency between the RB1 gene and two closely linked microsatellites using sperm typing, EUR J HUM G, 7(2), 1999, pp. 239-242

Authors: Coubes, P Echenne, B Roubertie, A Vayssiere, N Tuffery, S Humbertclaude, V Cambonie, G Claustres, M Frerebeau, P
Citation: P. Coubes et al., Treatment of early-onset generalized dystonia by bilateral chronic electrical stimulation of the internal globus pallidus. Case report., NEUROCHIRE, 45(2), 1999, pp. 139-144
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