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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 – 6 of 6 1 Thalamo-cortical network hyperconnectivity in preclinical progranulin mutation carriers. Lee, Suzee E; Sias, Ana C; Kosik, Eena L. - : eScholarship, University of California, 2019 BASE Show details 2 Thalamo-cortical network hyperconnectivity in preclinical progranulin mutation carriers. Lee, Suzee E; Sias, Ana C; Kosik, Eena L. - : eScholarship, University of California, 2019 BASE Show details 3 The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition. Hippolyte, L.; Maillard, A.M.; Rodriguez-Herreros, B.... In: Biological psychiatry, vol. 80, no. 2, pp. 129-139 (2016) BASE Show details 4 A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders. Zufferey, F.; Sherr, E.H.; Beckmann, N.D.... In: Journal of Medical Genetics, vol. 49, no. 10, pp. 660-668 (2012) BASE Show details 5 Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits. Groszer, M; Keays, DA; Deacon, RM... 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 (2008) BASE Show details 6 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

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