Functional characterisation of FOXP1 mutations found in patients with 
intellectual disability.

Derizioti, Pelagia; Fröhlich, Henning; Dimitropoulou, Danai; Rappold, Gudrun; Fisher, Simon E.

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Functional characterisation of FOXP1 mutations found in patients with intellectual disability.

Derizioti, P., Fröhlich, H., Dimitropoulou, D., Rappold, G., & Fisher, S. E. (2012). Functional characterisation of FOXP1 mutations found in patients with intellectual disability. Poster presented at New Frontiers Symposium in Personal Genomics, Nijmegen, the Netherlands.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-000E-7ECC-9 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0028-D363-2

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Creators:
Derizioti, Pelagia¹, Author
Fröhlich, Henning², Author
Dimitropoulou, Danai¹, Author
Rappold, Gudrun², Author
Fisher, Simon E.^{1, 3}, Author

Affiliations:
1Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, the Netherlands, ou_persistent22
2Department of Molecular Human Genetics, Ruprecht-Karls-University, Heidelberg, Germany, ou_persistent22
3Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, the Netherlands, ou_persistent22

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Dates: Created: 2012

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Title: New Frontiers Symposium in Personal Genomics

Place of Event: Nijmegen, the Netherlands

Start-/End Date: 2012-12-03 - 2012-12-04

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