Authors: Couvert, P Bienvenu, T Aquaviva, C Poirier, K Moraine, C Gendrot, C Verloes, A Andres, C Le Fevre, AC Souville, I Steffann, J des Portes, V Ropers, HH Yntema, HG Fryns, JP Briault, S Chelly, J Cherif, B

Citation: P. Couvert et al., MECP2 is highly mutated in X-linked mental retardation, HUM MOL GEN, 10(9), 2001, pp. 941-946

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