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Genome-wide association study of word reading: Overlap with risk genes for neurodevelopmental disorders.
Price, Kaitlyn M; Wigg, Karen G; Feng, Yu; Blokland, Kirsten; Wilkinson, Margaret; He, Gengming; Kerr, Elizabeth N; Carter, Tasha-Cate; Guger, Sharon L; Lovett, Maureen W; Strug, Lisa J; Barr, Cathy L.
  • Price KM; Genetics and Development Division, Krembil Research Institute, University Health Network, Toronto, Ontario, Canada.
  • Wigg KG; Program in Neuroscience and Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Feng Y; Department of Physiology, University of Toronto, Toronto, Ontario, Canada.
  • Blokland K; Genetics and Development Division, Krembil Research Institute, University Health Network, Toronto, Ontario, Canada.
  • Wilkinson M; Genetics and Development Division, Krembil Research Institute, University Health Network, Toronto, Ontario, Canada.
  • He G; Program in Neuroscience and Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Kerr EN; Program in Neuroscience and Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Carter TC; Genetics and Genome Biology, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Guger SL; Department of Psychology, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Lovett MW; Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada.
  • Strug LJ; Program in Neuroscience and Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Barr CL; Holland Bloorview Rehabilitation Hospital, Toronto, Ontario, Canada.
Genes Brain Behav ; 19(6): e12648, 2020 07.
Article en En | MEDLINE | ID: mdl-32108986
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Lectura / Trastorno por Déficit de Atención con Hiperactividad / Polimorfismo de Nucleótido Simple / Dislexia / Trastorno del Espectro Autista Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Female / Humans / Male Idioma: En Año: 2020 Tipo del documento: Article
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Lectura / Trastorno por Déficit de Atención con Hiperactividad / Polimorfismo de Nucleótido Simple / Dislexia / Trastorno del Espectro Autista Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Child / Female / Humans / Male Idioma: En Año: 2020 Tipo del documento: Article