A novel method for finding functional variants in whole exome sequencing 
reveals potential risk factors for specific language impairments

Ho, Joses; Chen, S.; Hoischen, A.; Devanna, Paolo; Francks, Clyde; SLI Consortium; Veltman, J. A.; Newbury, D. F.; Fisher, Simon E.; Vernes, Sonja C.

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A novel method for finding functional variants in whole exome sequencing reveals potential risk factors for specific language impairments

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Ho, Joses
Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society;
International Max Planck Research School for Language Sciences, MPI for Psycholinguistics, Max Planck Society, Nijmegen, NL;

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Devanna, Paolo
Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society;

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Francks, Clyde
Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society;

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Fisher, Simon E.
Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society;

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Vernes, Sonja C.
Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society;

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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.

引用: https://hdl.handle.net/11858/00-001M-0000-0014-5B55-7

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