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