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Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.
Chen, Xiaowei Sylvia; Reader, Rose H; Hoischen, Alexander; Veltman, Joris A; Simpson, Nuala H; Francks, Clyde; Newbury, Dianne F; Fisher, Simon E.
Affiliation
  • Chen XS; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.
  • Reader RH; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.
  • Hoischen A; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Veltman JA; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Simpson NH; Department of Clinical Genetics, University of Maastricht, Maastricht, The Netherlands.
  • Francks C; Donders Institute for Brain, Cognition and Behaviour, Nijmegen, The Netherlands.
  • Newbury DF; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.
  • Fisher SE; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.
Sci Rep ; 7: 46105, 2017 04 25.
Article in En | MEDLINE | ID: mdl-28440294
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Full text: 1 Database: MEDLINE Main subject: Genetic Predisposition to Disease / High-Throughput Nucleotide Sequencing / Language Development Disorders / Mutation Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Year: 2017 Type: Article
Fulltext
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Full text: 1 Database: MEDLINE Main subject: Genetic Predisposition to Disease / High-Throughput Nucleotide Sequencing / Language Development Disorders / Mutation Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Year: 2017 Type: Article