Horn, D., J. Kapeller, N. Rivera-Brugues, U. Moog, B. Lorenz-Depiereux, S. Eck, M. Hempel, J. Wagenstaller, A. Gawthrope, A. P. Monaco, M. Bonin, O. Riess, E. Wohlleber, T. Illig, C. R. Bezzina, A. Franke, S. Spranger, P. Villavicencio-Lorini, W. Seifert, J. Rosenfeld, E. Klopocki, G. A. Rappold and T. M. Strom: Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. In: Human Mutation 31, 11, E1851-E1860 (2010).
url: http://www.ncbi.nlm.nih.gov/pubmed/20848658
doi: 10.1002/humu.21362
Seifert, W., M. Holder-Espinasse, S. Spranger, M. Hoeltzenbein, E. Rossier, H. Dollfus, H. Lacombe, A. Verloes, K. H. Chrzanowska, G. H. B. Maegawa, D. Chitayat, D. Kotzot, D. Huhle, P. Meinecke, B. Albrecht, I. Mathijssen, B. Leheup, K. Raile, H. C. Hennies and D. Horn: Mutational spectrum of COH1 and clinical heterogeneity in Cohen syndrome. In: Journal of Medical Genetics 43, 5, e22-e22 (2006).
doi: 10.1136/jmg.2005.039867
http://edoc.mpg.de
The Max Planck Society does not take any responsibility for the content of this export.