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

Year Number of Results
1989 2
1991 2
1993 2
1994 1
1995 1
1996 1
1997 2
1999 4
2000 9
2001 6
2002 9
2003 16
2004 22
2005 20
2006 25
2007 26
2008 58
2009 75
2010 77
2011 86
2012 73
2013 61
2014 56
2015 71
2016 63
2017 57
2018 41
2019 25
2020 7
2021 2
2022 2
2023 2
2024 0

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My NCBI Collection - Speech and Language Pathology View in My NCBI

794 results

Results by year

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Page 1
FOXP2-Related Speech and Language Disorder.
Morgan A, Fisher SE, Scheffer I, Hildebrand M. Morgan A, et al. 2016 Jun 23 [updated 2023 Jan 26]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2016 Jun 23 [updated 2023 Jan 26]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 27336128 Free Books & Documents. Review.
Severe speech impairment is a distinguishing feature of FOXP1-related disorder.
Braden RO, Amor DJ, Fisher SE, Mei C, Myers CT, Mefford H, Gill D, Srivastava S, Swanson LC, Goel H, Scheffer IE, Morgan AT. Braden RO, et al. Dev Med Child Neurol. 2021 Dec;63(12):1417-1426. doi: 10.1111/dmcn.14955. Epub 2021 Jun 9. Dev Med Child Neurol. 2021. PMID: 34109629 Free article.
Primate auditory prototype in the evolution of the arcuate fasciculus.
Balezeau F, Wilson B, Gallardo G, Dick F, Hopkins W, Anwander A, Friederici AD, Griffiths TD, Petkov CI. Balezeau F, et al. Nat Neurosci. 2020 May;23(5):611-614. doi: 10.1038/s41593-020-0623-9. Epub 2020 Apr 20. Nat Neurosci. 2020. PMID: 32313267 Free PMC article.
794 results