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

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.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-5B55-7 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-7575-7

Genre: Poster

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Creators:
Ho, Joses^{1, 2}, Author
Chen, S., Author
Hoischen, A., Author
Devanna, Paolo¹, Author
Francks, Clyde¹, Author
SLI Consortium, Author
Veltman, J. A., Author
Newbury, D. F., Author
Fisher, Simon E.¹, Author
Vernes, Sonja C.¹, Author

Affiliations:
1Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society, ou_792549
2International Max Planck Research School for Language Sciences, MPI for Psycholinguistics, Max Planck Society, Nijmegen, NL, ou_1119545

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Language(s): eng - English

Dates: Created: 2013

Publication Status: Not specified

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Title: the Cognomics Symposium 2013

Place of Event: Nijmegen, The Netherlands

Start-/End Date: 2013-09-10 - 2013-09-11

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