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  Genome-wide screening for DNA variants associated with dyslexia and language impairment

Gialluisi, A., Newbury, D. F., Wilcutt, E. G., Olson, R. K., Brandler, W. M., Paracchini, S., et al. (2012). Genome-wide screening for DNA variants associated with dyslexia and language impairment. Poster presented at the New Frontiers Symposium 2012: Genomics in health and disease - Towards personal genomics, Nijmegen, The Netherlands.

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 Creators:
Gialluisi, Alessandro1, 2, Author           
Newbury, D. F., Author
Wilcutt, E. G., Author
Olson, R. K., Author
Brandler, W. M., Author
Paracchini, S., Author
Monaco, A. P., Author
Francks, Clyde1, Author           
Fisher, Simon E.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: 2012
 Publication Status: Not specified
 Pages: -
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 Table of Contents: -
 Rev. Type: -
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Title: the New Frontiers Symposium 2012: Genomics in health and disease - Towards personal genomics
Place of Event: Nijmegen, The Netherlands
Start-/End Date: 2012-12-03 - 2012-12-04

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