Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
Horn D, Illig T, Bezzina C, Franke A, Spranger S, Villavicencio-Lorini P, Seifert W, Rosenfeld J, Klopocki E, Rappold G, Wohlleber E, Riess O, Bonin M, Kapeller J, Rivera-Brugués N, Moog U, Lorenz-Depiereux B, Eck S, Hempel M, Wagenstaller J, Gawthrope A, Monaco A, Strom T. Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. Hum Mutat 2010; 31:E1851-60.
Nov 1, 2010
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
Nov 1, 2010
Hum Mutat 2010; 31:E1851-60
Horn Denise, Illig Thomas, Bezzina Connie R, Franke Andre, Spranger Stephanie, Villavicencio-Lorini Pablo, Seifert Wenke, Rosenfeld Jochen, Klopocki Eva, Rappold Gudrun A, Wohlleber Eva, Riess Olaf, Bonin Michael, Kapeller Johannes, Rivera-Brugués Núria, Moog Ute, Lorenz-Depiereux Bettina, Eck Sebastian, Hempel Maja, Wagenstaller Janine, Gawthrope Alex, Monaco Anthony P, Strom Tim M
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