Genome-wide analysis identifies a role for common copy number variants in specific language impairment.
Saved in:
| Title: | Genome-wide analysis identifies a role for common copy number variants in specific language impairment. |
|---|---|
| Authors: | Simpson NH; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK., Ceroni F; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK., Reader RH; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK., Covill LE; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK., Knight JC; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK., Hennessy ER; University Child Health and DMDE, University of Aberdeen, Aberdeen, UK., Bolton PF; Departments of Child and Adolescent Psychiatry, Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, King's College London, London, UK., Conti-Ramsden G; School of Psychological Sciences, University of Manchester, Manchester, UK., O'Hare A; Department of Reproductive and Developmental Sciences, University of Edinburgh, Edinburgh, UK., Baird G; Children's Neurosciences Department, Evelina Children's Hospital and King's Health Partners, London, UK., Fisher SE; Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands., Newbury DF; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.; St John's College, University of Oxford, Oxford, UK. |
| Corporate Authors: | SLI Consortium |
| Source: | European journal of human genetics : EJHG [Eur J Hum Genet] 2015 Oct; Vol. 23 (10), pp. 1370-7. Date of Electronic Publication: 2015 Jan 14. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
Be the first to leave a comment!
