C. Lai

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.

N. Sykes, A. Monaco, F. Vargha-Khadem, 2005, American journal of human genetics.

Molecular evolution of FOXP2, a gene involved in speech and language

A. Monaco, S. Pääbo, W. Enard, 2002, Nature.

A forkhead-domain gene is mutated in a severe speech and language disorder

A. Monaco, F. Vargha-Khadem, S. Fisher, 2001, Nature.