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Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees.
Woodbury-Smith, Marc; Zarrei, Mehdi; Wei, John; Thiruvahindrapuram, Bhooma; O'Connor, Irene; Paterson, Andrew D; Yuen, Ryan K C; Dastan, Jila; Stavropoulos, Dimitri J; Howe, Jennifer L; Thompson, Ann; Parlier, Morgan; Fernandez, Bridget; Piven, Joseph; Anagnostou, Evdokia; Scherer, Stephen W; Vieland, Veronica J; Szatmari, Peter.
Afiliación
  • Woodbury-Smith M; Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.
  • Zarrei M; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Wei J; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Thiruvahindrapuram B; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • O'Connor I; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Paterson AD; Department of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, Ontario, Canada.
  • Yuen RKC; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Dastan J; Division of Epidemiology and Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
  • Stavropoulos DJ; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Howe JL; Department of Paediatric Laboratory Medicine, Molecular Genetics Laboratory, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Thompson A; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Parlier M; Department of Paediatric Laboratory Medicine, Molecular Genetics Laboratory, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Fernandez B; The Centre for Applied Genomics, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Piven J; Department of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, Ontario, Canada.
  • Anagnostou E; Carolina Institute for Developmental Disabilities, University of North Carolina at Chapel Hill, School of Medicine, Chapel Hill, North Carolina, USA.
  • Scherer SW; Provincial Medical Genetics Program, Health Sciences Center, St. John's, Newfoundland, Canada.
  • Vieland VJ; Carolina Institute for Developmental Disabilities, University of North Carolina at Chapel Hill, School of Medicine, Chapel Hill, North Carolina, USA.
  • Szatmari P; Holland Bloorview Hospital, Toronto, Ontario, Canada.
Am J Med Genet B Neuropsychiatr Genet ; 183(5): 268-276, 2020 07.
Article en En | MEDLINE | ID: mdl-32372567
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Linaje / Análisis Mutacional de ADN / Dosificación de Gen / Variaciones en el Número de Copia de ADN / Trastorno del Espectro Autista Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Am J Med Genet B Neuropsychiatr Genet Asunto de la revista: GENETICA MEDICA / NEUROLOGIA / PSIQUIATRIA Año: 2020 Tipo del documento: Article País de afiliación: Reino Unido
Texto completo
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PubMed Links
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Linaje / Análisis Mutacional de ADN / Dosificación de Gen / Variaciones en el Número de Copia de ADN / Trastorno del Espectro Autista Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Am J Med Genet B Neuropsychiatr Genet Asunto de la revista: GENETICA MEDICA / NEUROLOGIA / PSIQUIATRIA Año: 2020 Tipo del documento: Article País de afiliación: Reino Unido