Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits
The American Journal of Human Genetics2005Vol. 76(6), pp. 1074–1080
Citations Over TimeTop 10% of 2005 papers
Kay MacDermot, Elena Bonora, Nuala Sykes, Anne-Marie Coupe, Cecilia Lai, Sonja C. Vernes, Faraneh Vargha‐Khadem, Fiona McKenzie, Robert L. Smith, Anthony P. Monaco, Simon E. Fisher
Related Papers
- → Association of Specific Language Impairment (SLI) to the Region of 7q31(2003)114 cited
- → Recent advances in the genetics of language impairment(2010)101 cited
- → Language-impaired children: No sign of the FOXP2 mutation(2002)64 cited
- → Speech disruptions in pre-school children with specific language impairment and phonological impairment(1999)15 cited
- → Genetics of Specific Language Impairment(2009)