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  Discovery of genome-wide significant risk loci for dyslexia

Doust, C., Fontanillas, P., Eising, E., Gordon, S. D., GenLang Consortium, Martin, N. G., et al. (2020). Discovery of genome-wide significant risk loci for dyslexia. Poster presented at the World Congress of Psychiatric Genetics (WCPG 2020), online.

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 Creators:
Doust, Catherine1, Author
Fontanillas, Pierre2, Author
Eising, Else3, Author           
Gordon, Scott D.4, Author
GenLang Consortium, Author              
Martin, Nicholas G.4, Author
Bates, Timothy C.1, Author
Fisher, Simon E.3, 5, Author           
Luciano, Michelle1, Author
Affiliations:
1Department of Psychology, The University of Edinburgh, Edinburgh, EH8 9JZ, Scotland, ou_persistent22              
223andMe, ou_persistent22              
3Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society, ou_792549              
4Genetic Epidemiology Laboratory, QIMR Berghofer Medical Research Institute, Brisbane 4029, Queensland, Australia, ou_persistent22              
5Donders Institute for Brain, Cognition and Behaviour, Nijmegen, The Netherlands, ou_persistent22              

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 Dates: 2020
 Publication Status: Not specified
 Pages: -
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Title: the World Congress of Psychiatric Genetics (WCPG 2020)
Place of Event: online
Start-/End Date: 2020-10-19 - 2020-10-22

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