Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. by Horn, D, Kapeller, J, Rivera-Brugués, N, Moog, U, Lorenz-Depiereux, B, Eck, S, Hempel, M, Wagenstaller, J, Gawthrope, A, Monaco, A, Bonin, M, Riess, O, Wohlleber, E, Illig, T, Bezzina, C, Franke, A, Spranger, S, Villavicencio-Lorini, P, Seifert, W, Rosenfeld, J, Klopocki, E, Rappold, G, Strom, T

Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing by Nicod, J, Davies, R, Cai, N, Hassett, C, Goodstadt, L, Cosgrove, C, Yee, B, Lionikaite, V, McIntyre, R, Remme, C, Lodder, E, Gregory, J, Hough, T, Joynson, R, Phelps, H, Nell, B, Rowe, C, Wood, J, Walling, A, Bopp, N, Bhomra, A, Hernandez-Pliego, P, Callebert, J, Aspden, R, Talbot, N, Robbins, P, Harrison, M, Fray, M, Launay, J, Pinto, Y, Blizard, D, Bezzina, C, Adams, D, Franken, P, Weaver, T, Wells, S, Brown, S, Potter, P, Klenerman, P, Lionikas, A, Mott, R, Flint, J