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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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 Creators:
Ho, Joses1, 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: 2013
 Publication Status: Not specified
 Pages: -
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 Table of Contents: -
 Rev. Type: -
 Identifiers: -
 Degree: -

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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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