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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. Among authors: fisher se. 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.
Decoding the genetics of speech and language.
Graham SA, Fisher SE. Graham SA, et al. Among authors: fisher se. Curr Opin Neurobiol. 2013 Feb;23(1):43-51. doi: 10.1016/j.conb.2012.11.006. Epub 2012 Dec 7. Curr Opin Neurobiol. 2013. PMID: 23228431 Review.
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.
Simpson NH, Addis L, Brandler WM, Slonims V, Clark A, Watson J, Scerri TS, Hennessy ER, Bolton PF, Conti-Ramsden G, Fairfax BP, Knight JC, Stein J, Talcott JB, O'Hare A, Baird G, Paracchini S, Fisher SE, Newbury DF; SLI Consortium. Simpson NH, et al. Among authors: fisher se. Dev Med Child Neurol. 2014 Apr;56(4):346-53. doi: 10.1111/dmcn.12294. Epub 2013 Oct 9. Dev Med Child Neurol. 2014. PMID: 24117048 Free PMC article.
Foxp1/2/4 regulate endochondral ossification as a suppresser complex.
Zhao H, Zhou W, Yao Z, Wan Y, Cao J, Zhang L, Zhao J, Li H, Zhou R, Li B, Wei G, Zhang Z, French CA, Dekker JD, Yang Y, Fisher SE, Tucker HO, Guo X. Zhao H, et al. Among authors: fisher se. Dev Biol. 2015 Feb 15;398(2):242-54. doi: 10.1016/j.ydbio.2014.12.007. Epub 2014 Dec 17. Dev Biol. 2015. PMID: 25527076 Free PMC article.
Speech and Language: Translating the Genome.
Deriziotis P, Fisher SE. Deriziotis P, et al. Among authors: fisher se. Trends Genet. 2017 Sep;33(9):642-656. doi: 10.1016/j.tig.2017.07.002. Epub 2017 Aug 3. Trends Genet. 2017. PMID: 28781152 Review.
408 results