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Reply to Pembrey et al: ‘ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis’

MPS-Authors
/persons/resource/persons4382

Francks,  Clyde
Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society;
Donders Institute for Brain, Cognition and Behaviour, External Organizations;
Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK;
Imaging Genomics, MPI for Psycholinguistics, Max Planck Society;

Martin,  Hilary
Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society;

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

SLI Consortium, 
Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society;

WGS500 Consortium, 
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;
Donders Institute for Brain, Cognition and Behaviour, External Organizations;

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Fulltext (public)

Ceroni_etal_2015.pdf
(Publisher version), 307KB

Supplementary Material (public)
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Citation

Ceroni, F., Simpson, N. H., Francks, C., Baird, G., Conti-Ramsden, G., Clark, A., et al. (2015). Reply to Pembrey et al: ‘ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis’. European Journal of Human Genetics, 23, 1113-1115. doi:10.1038/ejhg.2014.275.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0024-90ED-5
Abstract
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