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Neurodevelopmental functioning in probands and non-proband carriers of 22q11.2 microduplication.
Drmic, Irene E; MacKinnon Modi, Bonnie; McConnell, Beth; Jilderda, Sanne; Hoang, Ny; Noor, Abdul; Bassett, Anne S; Speevak, Marsha; Stavropoulos, Dimitri J; Carter, Melissa T.
  • Drmic IE; McMaster Children's Hospital Autism Program, Ron Joyce Children's Health Centre, Hamilton Health Sciences, Hamilton, Ontario, Canada.
  • MacKinnon Modi B; Autism Research Unit, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • McConnell B; Autism Research Unit, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Jilderda S; Autism Research Centre, Glenrose Rehabilitation Hospital, Edmonton, Alberta, Canada.
  • Hoang N; Autism Research Unit, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Noor A; Department of Genetic Counselling, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Bassett AS; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.
  • Speevak M; Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, Ontario, Canada.
  • Stavropoulos DJ; The Daglish Family 22q Clinic, Toronto, Ontario, Canada.
  • Carter MT; Department of Laboratory Medicine and Genetics, Trillium Health Partners, Credit Valley Site, Toronto, Ontario, Canada.
Am J Med Genet A ; 188(10): 2999-3008, 2022 10.
Article en En | MEDLINE | ID: mdl-35899837

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Síndrome de DiGeorge / Trastorno del Espectro Autista Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Síndrome de DiGeorge / Trastorno del Espectro Autista Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article