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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 Page: 1 2 Hits 1 – 20 of 32 1 Spatially explicit analysis reveals complex human genetic gradients in the Iberian Peninsula Pimenta, J; Lopes, AM; Carracedo, A. - : Nature Publishing Group, 2019 BASE Show details 2 7p22.1 microduplication syndrome: Refinement of the critical region. Ronzoni, L; Grassi, FS; Pezzani, L. - 2017 BASE Show details 3 A human neurodevelopmental model for Williams syndrome. Chailangkarn, Thanathom; Trujillo, Cleber A; Freitas, Beatriz C... In: Nature, vol 536, iss 7616 (2016) BASE Show details 4 A human neurodevelopmental model for Williams syndrome. Chailangkarn, Thanathom; Trujillo, Cleber A; Freitas, Beatriz C... In: Nature, vol 536, iss 7616 (2016) BASE Show details 5 Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families. Leppa, Virpi M; Kravitz, Stephanie N; Martin, Christa Lese... In: American journal of human genetics, vol 99, iss 3 (2016) BASE Show details 6 Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities. D'Angelo, D.; Lebon, S.; Chen, Q.... In: Jama Psychiatry, vol. 73, no. 1, pp. 20-30 (2016) BASE Show details 7 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 8 A novel multi-alignment pipeline for high-throughput sequencing data. Huang, Shunping; Holt, James; Kao, Chia-Yu... In: Database : the journal of biological databases and curation, vol 2014, iss 0 (2014) BASE Show details 9 Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia. Simpson, NH; Addis, L; Brandler, WM... 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 (2014) BASE Show details 10 Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. Nudel, R; Simpson, NH; Baird, G... 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 (2014) BASE Show details 11 TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities. Wiszniewski, W; Hunter, JV; Hanchard, NA... 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 (2013) BASE Show details 12 Demographic histories, isolation and social factors as determinants of the genetic structure of Alpine linguistic groups Coia, V; Capocasa, M; Anagnostou, P. - 2013 BASE Show details 13 New insight on the Xq28 association with systemic sclerosis. Carmona, FD; Cénit, MC; Diaz-Gallo, LM... In: Ann Rheum Dis , 72 (12) 2032 - 2038. (2013) (2013) BASE Show details 14 Deletion of chromosome 12q21 affecting KCNC2 and ATXN7L3B in a family with neurodevelopmental delay and ataxia. Rajakulendran, S; Roberts, J; Koltzenburg, M... In: J Neurol Neurosurg Psychiatry , 84 (11) 1255 - 1257. (2013) (2013) BASE Show details 15 Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level. Barber, JC; Maloney, V; Hollox, EJ... In: PubMed ; http://www.ncbi.nlm.nih.gov/pubmed/ (2012) BASE Show details 16 Clan, language, and migration history has shaped genetic diversity in Haida and Tlingit populations from southeast Alaska Schurr, T.; Dulik, M.; Owings, A.. - : Wiley-Liss, 2012 BASE Show details 17 Migration distance rather than migration rate explains genetic diversity in human patrilocal groups. Marks, SJ; Levy, H; Martinez-Cadenas, C... 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 (2012) BASE Show details 18 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 19 Communication theory and multicellular biology. Mian, IS; Rose, C In: Integr Biol (Camb) , 3 (4) 350 - 367. (2011) (2011) BASE Show details 20 Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population. Villanueva, P; Newbury, DF; Jara, L... 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 (2011) BASE Show details Page: 1 2

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