English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
Add to Basket
  Local TagsRelease HistoryDetailsSummary

Released
Poster

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

MPS-Authors
/persons/resource/persons71886

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;

/persons/resource/persons41443

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

/persons/resource/persons4382

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

/persons/resource/persons4427

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

/persons/resource/persons37905

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

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
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: https://hdl.handle.net/11858/00-001M-0000-0014-5B55-7
Abstract
There is no abstract available