FOXP2

Publications

Fee EJ. The phonological system of a specifically language-impaired population. Clin Linguist Phon. 1995;9:189– 209. PMID: 21749311.

Feuk L et al. Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia. Am J Hum Genet. 2006;79:965–72. PMID: 17033973.

Fisher SE et al. Localisation of a gene implicated in a severe speech and language disorder. Nat Genet. 1998;18:168–70. PMID: 9462748.

Fisher SE et al. FOXP2 as a molecular window into speech and language. Trends Genet. 2009;25(4):166-77. PMID: 19304338.

Lai CS et al. A forkhead-domain gene is mutated in a severe speech and language disorder. Nature. 2001;413:519–23. PMID: 11586359.

Liégeois FJ et al. Early neuroimaging markers of FOXP2 intragenic deletion. Sci Rep. 2016;6:35192. PMID: 27734906.

Lennon PA et al. Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review. Am J Med Genet A. 2007;143A:791–8. PMID: 17330859.

MacDermot KD et al. Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. Am J Hum Genet. 2005;76:1074–80. PMID: 15877281.

Morgan AT et al. FOXP2-related speech and language disorders. Gene Reviews. 2017. PMID: 27336128.

Morgan AT et al. Interventions for childhood apraxia of speech. Cochrane Database ofSystematic Reviews. 2018. 29845607.

Palka C et al. Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. Pediatrics. 2012;129:e183–8. PMID: 22144704.

Rice GM et al. Phenotype of FOXP2 haploinsufficiency in a mother and son. Am J Med Genet A. 2012;158A:174–81. PMID: 22106036.

Reuter MS et al. FOXP2 variants in 14 individuals with developmental speech and language disorders broaden the mutational and clinical spectrum. J Med Genet. 2017;54:64–72. PMID: 27572252.

Turner SJ et al. Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria. Am J Med Genet A. 2013;161A:2321–6. PMID: 23918746.

Vargha-Khadem F et al. FOXP2 and the neuroanatomy of speech and language. Nat Rev Neurosci. 2005;6:131–8. PMID: 15685218.

Watkins KE et al. Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia. Brain. 2002;125:452–64. PMID: 11872604.

Zeesman S et al. Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2. Am J Med Genet A. 2006;140:509–14. PMID: 16470794.

Zilina O et al. Maternally and paternally inherited deletion of 7q31 involving the FOXP2 gene in two families. Am J Med Genet A. 2012;158A:254–6. PMID: 22105961.