Authors:
Zemni, R
Bienvenu, T
Vinet, MC
Sefiani, A
Carrie, A
Billuart, P
McDonell, N
Couvert, P
Francis, F
Chafey, P
Fauchereau, F
Friocourt, G
des Portes, V
Cardona, A
Frints, S
Meindl, A
Brandau, O
Ronce, N
Moraine, C
van Bokhoven, H
Ropers, HH
Sudbrak, R
Kahn, A
Fryns, JP
Beldjord, R
Chelly, J
Citation: R. Zemni et al., A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation, NAT GENET, 24(2), 2000, pp. 167-170
Authors:
Raynaud, M
Moizard, MP
Dessay, B
Briault, S
Toutain, A
Gendrot, C
Ronce, N
Moraine, C
Citation: M. Raynaud et al., Systematic analysis of X-inactivation in 19XLMR families: extremely skewedprofiles in carriers in three families, EUR J HUM G, 8(4), 2000, pp. 253-258
Authors:
des Portes, V
Beldjord, C
Chelly, J
Hamel, B
Kremer, H
Smits, A
van Bokhoven, H
Ropers, HH
Claes, S
Fryns, JP
Ronce, N
Gendrot, C
Toutain, A
Raynaud, M
Moraine, C
Citation: V. Des Portes et al., X-linked nonspecific mental retardation (MRX) linkage studies in 25 unrelated families: The European XLMR Consortium, AM J MED G, 85(3), 1999, pp. 263-265
Authors:
Gendrot, C
Ronce, N
Raynaud, M
Ayrault, AD
Dourlens, J
Castelnau, P
Muh, JP
Chelly, J
Moraine, C
Citation: C. Gendrot et al., X-linked nonspecific mental retardation (MRX16) mapping to distal Xq28: Linkage study and neuropsychological data in a large family, AM J MED G, 83(5), 1999, pp. 411-418
Authors:
Ronce, N
Raynaud, M
Toutain, A
Moizard, MP
Colleaux, L
Gendrot, C
Briault, S
Moraine, C
Citation: N. Ronce et al., Evidence for a new X-linked mental retardation gene in Xp21-Xp22: Clinicaland molecular data in one family, AM J MED G, 83(2), 1999, pp. 132-137