A novel method for finding functional variants in whole exome sequencing reveals potential risk factors for specific language impairments
Ho, J., Chen, S., Hoischen, A., Devanna, P., Francks, C., SLI Consortium, Veltman, J. A., Newbury, D. F., Fisher, S. E., & Vernes, S. C.
(2013). A novel method for finding functional variants in whole exome sequencing reveals potential risk factors for specific language impairments. Poster presented at the Cognomics Symposium 2013, Nijmegen, The Netherlands.
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