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Entries: 1-3  
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Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
Authors: Horn, D.; Kapeller, J.; Rivera-Brugues, N.; Moog, U.; Lorenz-Depiereux, B.; Eck, S.; Hempel, M.; Wagenstaller, J.; Gawthrope, A.; Monaco, A. P.; Bonin, M.; Riess, O.; Wohlleber, E.; Illig, T.; Bezzina, C. R.; Franke, A.; Spranger, S.; Villavicencio-Lorini, P.; Seifert, W.; Rosenfeld, J.; Klopocki, E.; Rappold, G. A.; Strom, T. M.
Date of Publication (YYYY-MM-DD): 2010-11-01
Title of Journal: Human Mutation
Volume: 31
Issue / Number: 11
Start Page: E1851
End Page: E1860
Document Type: Article
ID: 539476.0
 
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LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia
Authors: Francks, C.; Maegawa, S.; Lauren, J.; Abrahams, B. S.; Velayos-Baeza, A.; Medland, S. E.; Colella, S.; Groszer, Matthias; McAuley, E. Z.; Caffrey, T. M.; Timmusk, T.; Pruunsild, P.; Koppel, I.; Lind, P. A.; Matsumoto-Itaba, N.; Nicod, Jérôme; Xiong, L.; Joober, R.; Enard, Wolfgang; Krinsky, B.; Nanba, E.; Richardson, A. J.; Riley, B. P.; Martin, N. G.; Strittmatter, S. M.; Möller, H.-J.; Rujescu, D.; Clair, D. S.; Muglia, P.; Roos, L.; Fisher, Simon E.; Wade-Martins, R.; Rouleau, G. A.; Stein, J. F.; Karayiorgou, M.; Geschwind, D. H.; Ragoussis, J.; Kendler, K. S.; Airaksinen, M. S.; Oshimura, M.; DeLisi, L. E.; Monaco, A. P.
Date of Publication (YYYY-MM-DD): 2007
Title of Journal: Molecular Psychiatry
Volume: 12
Issue / Number: 12
Start Page: 1129
End Page: 1139
Document Type: Article
ID: 330762.0
Molecular evolution of FOXP2, a gene involved in speech and language
Authors: Enard, Wolfgang; Przeworski, Molly; Fisher, Simon E.; Lai, C. S. L.; Wiebe, Victor; Kitano, Takashi; Monaco, A. P.; Pääbo, Svante
Date of Publication (YYYY-MM-DD): 2002-08-22
Title of Journal: Nature
Volume: 418
Issue / Number: 6900
Start Page: 869
End Page: 872
Document Type: Article
ID: 21672.0
Entries: 1-3  
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