A list of SLI Consortium members can be found in the Acknowledgements section.
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia
Version of Record online: 9 OCT 2013
© 2013 The Authors. Developmental Medicine & Child Neurology published by John Wiley & Sons Ltd on behalf of Mac Keith Press.
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Developmental Medicine & Child Neurology
Volume 56, Issue 4, pages 346–353, April 2014
How to Cite
Simpson, N. H., Addis, L., Brandler, W. M., Slonims, V., Clark, A., Watson, J., Scerri, T. S., Hennessy, E. R., Bolton, P. F., Conti-Ramsden, G., Fairfax, B. P., Knight, J. C., Stein, J., Talcott, J. B., O'Hare, A., Baird, G., Paracchini, S., Fisher, S. E., Newbury, D. F. and Consortium, S. (2014), Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia. Developmental Medicine & Child Neurology, 56: 346–353. doi: 10.1111/dmcn.12294
- Issue online: 14 MAR 2014
- Version of Record online: 9 OCT 2013
- Manuscript Accepted: 9 AUG 2013
- Medical Research Council. Grant Numbers: G1000569/1, MR/J003719/1
- Max Planck Society
- Wellcome Trust. Grant Numbers: 074318, 088891
- European Research Council under the European Union's Seventh Framework Programme. Grant Numbers: FP7/2007-2013, 281824
- National Institute for Health Research (NIHR) Oxford Biomedical Research Centre
- National Institute of Health Research (UK) Senior Investigator
- Biomedical Research Centre in Mental Health at the South London & Maudsley NHS Trust Hospital, London
- Wellcome Trust. Grant Number: 090532/Z/09/Z
|dmcn12294-sup-0001-FigS1.pdf||application/PDF||784K||Figure S1: Causative mechanisms of the sex chromosome aneuploidies.|
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