Generation of mice with a conditional Foxp2 null allele. by French, C, Groszer, M, Preece, C, Coupe, A, Rajewsky, K, Fisher, S

Functional genetic analysis of mutations implicated in a human speech and language disorder. by Vernes, S, Nicod, J, Elahi, F, Coventry, J, Kenny, N, Coupe, A, Bird, L, Davies, K, Fisher, S

Identification of foxp2 truncation as a novel cause of developmental speech disorder. by MacDermot, K, Bonora, E, Sykes, N, Coupe, A, Lai, C, Vargha-Khadem, F, McKenzie, F, Smith, R, Monaco, A, Fisher, S

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. by MacDermot, K, Bonora, E, Sykes, N, Coupe, A, Lai, C, Vernes, S, Vargha-Khadem, F, McKenzie, F, Smith, R, Monaco, A, Fisher, S