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Maternally and Paternally Inherited Deletion of 7q31 Involving the FOXP2 Gene in Two FamiliesZILINA, O; REIMAND, T; ZJABLOVSKAJA, P et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 1, pp 254-256, issn 1552-4825, 3 p.Article

Identification of the Transcriptional Targets of FOXP2, a Gene Linked to Speech and Language, in Developing Human BrainSPITERI, Elizabeth; KONOPKA, Genevieve; COPPOLA, Giovanni et al.American journal of human genetics. 2007, Vol 81, Num 6, pp 1144-1157, issn 0002-9297, 14 p.Article

High-Throughput Analysis of Promoter Occupancy Reveals Direct Neural Targets of FOXP2, a Gene Mutated in Speech and Language DisordersVERNES, Sonja C; SPITERI, Elizabeth; NICOD, Jérome et al.American journal of human genetics. 2007, Vol 81, Num 6, pp 1232-1250, issn 0002-9297, 19 p.Article

Language-impaired children: No sign of the FOXP2 mutationMEABURN, E; DALE, P. S; CRAIG, I. W et al.Neuroreport (Oxford). 2002, Vol 13, Num 8, pp 1075-1077, issn 0959-4965Article

¿Homo loquens neanderthalensis? En torno a las capacidades simbólicas y lingüísticas del Neandertal = Homo loquens neanderthalensis? On the symbolic and linguistic capacities of NeandertalsBALARI, Sergio; BENITEZ BURRACO, Antonio; CAMPS, Marta et al.Munibe. Antropologia-arkeologia. 2008, Num 59, pp 3-24, issn 1132-2217, 22 p.Article

Facteurs génétiques dans les troubles spécifiques du développement du langage : Dysphasie = Genetic factors in developmental speech and language disordersPHILIPPE, A.ANAE. Approche neuropsychologique des apprentissages chez l'enfant. 2004, Num 76-77, pp 34-37, issn 0999-792X, 4 p.Article

FOXP2 polymorphisms in patients with schizophreniaSANJUAN, Julio; TOLOSA, Amparo; GONZALEZ, Jose Carlos et al.Schizophrenia research. 2005, Vol 73, Num 2-3, pp 253-256, issn 0920-9964, 4 p.Article

The origins of modernity: Was autonomous speech the critical factor?CORBALLIS, Michael C.Psychological review. 2004, Vol 111, Num 2, pp 543-552, issn 0033-295X, 10 p.Article

Molecular evolution of FOXP2, a gene involved in speech and languageENARD, Wolfgang; PRZEWORSKI, Molly; FISHER, Simon E et al.Nature (London). 2002, Vol 418, Num 6900, pp 869-872, issn 0028-0836Article

A forkhead-domain gene is mutated in a severe speech and language disorderLAI, Cecllia S. L; FISHER, Simon E; HURST, Jane A et al.Nature (London). 2001, Vol 413, Num 6855, pp 519-523, issn 0028-0836Article

Genes, Brains, and Language : An Epistemological Examination of How Genes Can Underlie Human Cognitive BehaviorGONTIER, Nathalie.Review of general psychology. 2008, Vol 12, Num 2, pp 170-180, issn 1089-2680, 11 p.Conference Paper

Association between the FOXP2 gene and autistic disorder in Chinese populationXIAOHONG GONG; MEIXIANG JIA; DAI ZHANG et al.American journal of medical genetics. 2004, Vol 127B, Num 1, pp 113-116, issn 0148-7299, 4 p.Article

Evaluation of FOXP2 as an autism susceptibility geneWASSINK, Thomas H; PIVEN, Joseph; VIELAND, Veronica J et al.American journal of medical genetics. 2002, Vol 114, Num 5, pp 566-569, issn 0148-7299Article

Tangled webs : Tracing the connections between genes and cognitionFISHER, Simon E.Cognition. 2006, Vol 101, Num 2, pp 270-297, issn 0010-0277, 28 p.Article

FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorderLAI, Cecilia S. L; GERRELLI, Dianne; MONACO, Anthony P et al.Brain. 2003, Vol 126, pp 2455-2462, issn 0006-8950, 8 p., 11Article

Bilateral Brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxiaBELTON, Emma; SALMOND, Claire H; WATKINS, Kate E et al.Human brain mapping. 2003, Vol 18, Num 3, pp 194-200, issn 1065-9471, 7 p.Article

Modified sound-evoked brainstem potentials in Foxp2 mutant miceKURT, Simone; GROSZER, Matthias; FISHER, Simon E et al.Brain research. 2009, Vol 1289, pp 30-36, issn 0006-8993, 7 p.Article

Anomalies morphologiques et fonctionnelles du cerveau associées à une mutation du gène FOXP2 dans un trouble héréditaire de la parole et du langage = Morphological and functional brain abnormalities associated with a mutation of the FOXP2 gene in a hereditary speech and language disorderLIEGEOIS, Frédérique.Rééducation orthophonique. 2005, Vol 43, Num 223, pp 299-307, issn 0034-222X, 9 p.Conference Paper