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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Hits 1 – 4 of 4 1 Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. MacDermot, KD; Bonora, E; Sykes, N... In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2005) BASE Show details 2 Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits MacDermot, KD; Bonora, E; Sykes, N... In: American Journal of Human Genetics , 76 (6) pp. 1074-1080. (2005) (2005) BASE Show details 3 Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits MacDermot, KD; Bonora, E; Sykes, N... In: AM J HUM GENET , 76 (6) 1074 - 1080. (2005) (2005) BASE Show details 4 Identification of FOXP2 Truncation as a novel cause of developmental speech and language deficits MacDermot, K.D.; Bonora, E.; Sykes, N.... In: American Journal of Human Genetics , 76 (6) pp.1074 - 1080. (2005) (2005) BASE Show details

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