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Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities.
Price, Kaitlyn M; Wigg, Karen G; Eising, Else; Feng, Yu; Blokland, Kirsten; Wilkinson, Margaret; Kerr, Elizabeth N; Guger, Sharon L; Fisher, Simon E; Lovett, Maureen W; Strug, Lisa J; Barr, Cathy L.
Afiliación
  • Price KM; Division of Experimental and Translational Neuroscience, Krembil Research Institute, University Health Network, Toronto, Ontario, Canada.
  • Wigg KG; Program in Neuroscience and Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Eising E; Department of Physiology, University of Toronto, Toronto, Ontario, Canada.
  • Feng Y; Division of Experimental and Translational Neuroscience, Krembil Research Institute, University Health Network, Toronto, Ontario, Canada.
  • Blokland K; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.
  • Wilkinson M; Division of Experimental and Translational Neuroscience, Krembil Research Institute, University Health Network, Toronto, Ontario, Canada.
  • Kerr EN; Program in Neuroscience and Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Guger SL; Program in Neuroscience and Mental Health, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Fisher SE; Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada.
  • Lovett MW; Department of Psychology, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Barr CL; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.
Transl Psychiatry ; 12(1): 495, 2022 11 29.
Article en En | MEDLINE | ID: mdl-36446759
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dislexia / Trastorno del Espectro Autista Tipo de estudio: Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Transl Psychiatry Año: 2022 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dislexia / Trastorno del Espectro Autista Tipo de estudio: Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Transl Psychiatry Año: 2022 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Estados Unidos