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Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'.
Ceroni, Fabiola; Simpson, Nuala H; Francks, Clyde; Baird, Gillian; Conti-Ramsden, Gina; Clark, Ann; Bolton, Patrick F; Hennessy, Elizabeth R; Donnelly, Peter; Bentley, David R; Martin, Hilary; Parr, Jeremy; Pagnamenta, Alistair T; Maestrini, Elena; Bacchelli, Elena; Fisher, Simon E; Newbury, Dianne F.
Afiliação
  • Ceroni F; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Simpson NH; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Francks C; 1] Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands [2] Donders Institute for Brain, Cognition & Behaviour, Nijmegen, The Netherlands.
  • Baird G; Guy's & St Thomas NHS Foundation Trust, Newcomen Children's Neurosciences Centre, St Thomas' Hospital, London, UK.
  • Conti-Ramsden G; School of Psychological Sciences, The University of Manchester, Manchester, UK.
  • Clark A; Speech and Hearing Sciences, Queen Margaret University, Edinburgh, UK.
  • Bolton PF; Departments of Child & Adolescent Psychiatry & Social Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, Kings College London, London, UK.
  • Hennessy ER; University Child Health and DMDE, University of Aberdeen, Aberdeen, UK.
  • Donnelly P; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Bentley DR; Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Essex, UK.
  • Martin H; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Parr J; Institute of Neuroscience and Health and Society, Newcastle University, Newcastle upon Tyne, UK.
  • Pagnamenta AT; 1] Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK [2] NIHR Biomedical Research Centre, Oxford and Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Maestrini E; Dipartimento di Farmacia e Biotecnologie, University of Bologna, Bologna, Italy.
  • Bacchelli E; Dipartimento di Farmacia e Biotecnologie, University of Bologna, Bologna, Italy.
  • Fisher SE; 1] Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands [2] Donders Institute for Brain, Cognition & Behaviour, Nijmegen, The Netherlands.
  • Newbury DF; Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
Eur J Hum Genet ; 23(9): 1113-5, 2015 Sep.
Article em En | MEDLINE | ID: mdl-25537359
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Éxons / Deleção de Sequência / Proteínas de Ligação a DNA / Transtornos do Desenvolvimento da Linguagem Limite: Female / Humans / Male Idioma: En Revista: Eur J Hum Genet Ano de publicação: 2015 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Éxons / Deleção de Sequência / Proteínas de Ligação a DNA / Transtornos do Desenvolvimento da Linguagem Limite: Female / Humans / Male Idioma: En Revista: Eur J Hum Genet Ano de publicação: 2015 Tipo de documento: Article