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Journal: American Journal of Human Genetics 


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76(6) | 2005

MacDermot, K. D., Bonora, E., Sykes, N., Coupe, A., Lai, C. S., Vernes, S. C., Vargha-Khadem, F., McKenzie, F., Smith, R. L., Monaco, A. P. & Fisher, S. E. (2005) "Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits", American Journal of Human Genetics, 7 pages. doi: 10.1086/430841.

81(6) | 2007

Spiteri, E., Konopka, G., Coppola, G., Bomar, J., Oldham, M., Ou, J., Vernes, S. C., Fisher, S. E., Ren, B. & Geschwind, D. H. (2007) "Identification of the Transcriptional Targets of FOXP2, a Gene Linked to Speech and Language, in Developing Human Brain", American Journal of Human Genetics, 14 pages.



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