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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2012 4
2013 4
2014 5
2015 7
2016 4
2017 2
2018 2
2020 1
2021 1
2022 0
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28 results
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Page 1
The FOXP2-Driven Network in Developmental Disorders and Neurodegeneration.
Oswald F, Klöble P, Ruland A, Rosenkranz D, Hinz B, Butter F, Ramljak S, Zechner U, Herlyn H. Oswald F, et al. Front Cell Neurosci. 2017 Jul 26;11:212. doi: 10.3389/fncel.2017.00212. eCollection 2017. Front Cell Neurosci. 2017. PMID: 28798667 Free PMC article.
Genome-Wide Studies of Specific Language Impairment.
Reader RH, Covill LE, Nudel R, Newbury DF. Reader RH, et al. Curr Behav Neurosci Rep. 2014;1(4):242-250. doi: 10.1007/s40473-014-0024-z. Curr Behav Neurosci Rep. 2014. PMID: 25411653 Free PMC article. Review.
FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum.
Reuter MS, Riess A, Moog U, Briggs TA, Chandler KE, Rauch A, Stampfer M, Steindl K, Gläser D, Joset P; DDD Study, Krumbiegel M, Rabe H, Schulte-Mattler U, Bauer P, Beck-Wödl S, Kohlhase J, Reis A, Zweier C. Reuter MS, et al. J Med Genet. 2017 Jan;54(1):64-72. doi: 10.1136/jmedgenet-2016-104094. Epub 2016 Aug 29. J Med Genet. 2017. PMID: 27572252
28 results