Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits - Horn, Denise; Kapeller, Johannes; Rivera-Brugués, Núria; Moog, Ute; Lorenz-Depiereux, Bettina; Eck, Sebastian; Hempel, Maja; Wagenstaller, Janine; Gawthrope, Alex; Monaco, Anthony P.; Bonin, Michael; Riess, Olaf; et al. (Human mutation, 2010)
Published: 16 September 2010