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

MPS-Authors
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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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Citation

Ho, J., Chen, S., Hoischen, A., Devanna, P., Francks, C., SLI Consortium, et al. (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.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0014-5B55-7
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