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Atypical autism in a boy with double duplication of 22q11.2: implications of increasing dosage.
Dale, Breanne; Modi, Bonnie MacKinnon; Jilderda, Sanne; McConnell, Beth; Hoang, Ny; Swaroop, Pooja; Falcon, Jhoan; Thiruvahindrapuram, Bhooma; Walker, Susan; Scherer, Stephen W; Stavropoulos, D James; Drmic, Irene E; Carter, Melissa T.
Afiliación
  • Dale B; Autism Research Unit, The Hospital for Sick Children, Toronto, ON Canada.
  • Modi BM; Autism Research Unit, The Hospital for Sick Children, Toronto, ON Canada.
  • Jilderda S; Autism Research Unit, The Hospital for Sick Children, Toronto, ON Canada.
  • McConnell B; Autism Research Unit, The Hospital for Sick Children, Toronto, ON Canada.
  • Hoang N; Autism Research Unit, The Hospital for Sick Children, Toronto, ON Canada.
  • Swaroop P; The Centre for Applied Genomics, Hospital for Sick Children and McLaughlin Centre and Department of Molecular Genetics, University of Toronto, Toronto, ON Canada.
  • Falcon J; Autism Research Unit, The Hospital for Sick Children, Toronto, ON Canada.
  • Thiruvahindrapuram B; Autism Research Unit, The Hospital for Sick Children, Toronto, ON Canada.
  • Walker S; The Centre for Applied Genomics, Hospital for Sick Children and McLaughlin Centre and Department of Molecular Genetics, University of Toronto, Toronto, ON Canada.
  • Scherer SW; The Centre for Applied Genomics, Hospital for Sick Children and McLaughlin Centre and Department of Molecular Genetics, University of Toronto, Toronto, ON Canada.
  • Stavropoulos DJ; The Centre for Applied Genomics, Hospital for Sick Children and McLaughlin Centre and Department of Molecular Genetics, University of Toronto, Toronto, ON Canada.
  • Drmic IE; Department of Pathology and Laboratory Medicine, Genome Diagnostics, The Hospital for Sick Children, University of Toronto, Toronto, ON Canada.
  • Carter MT; Autism Research Unit, The Hospital for Sick Children, Toronto, ON Canada.
NPJ Genom Med ; 2: 28, 2017.
Article en En | MEDLINE | ID: mdl-29263838
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: NPJ Genom Med Año: 2017 Tipo del documento: Article
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: NPJ Genom Med Año: 2017 Tipo del documento: Article