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

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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.


Cite as: http://hdl.handle.net/11858/00-001M-0000-000E-7ECC-9
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