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Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome.
Fiksinski, Ania M; Schneider, Maude; Murphy, Clodagh M; Armando, Marco; Vicari, Stefano; Canyelles, Jaume M; Gothelf, Doron; Eliez, Stephan; Breetvelt, Elemi J; Arango, Celso; Vorstman, Jacob A S.
Afiliação
  • Fiksinski AM; Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Schneider M; Dalglish Family 22q Clinic for Adults with 22q11.2 Deletion Syndrome, Toronto General Hospital, University Health Network, and Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
  • Murphy CM; Developmental Imaging and Psychopathology Lab, Department of Psychiatry, School of Medicine, University of Geneva, Geneva, Switzerland.
  • Armando M; Center for Contextual Psychiatry, Department of Neurosciences, KU Leuven, Leuven, Belgium.
  • Vicari S; Sackler Institute for Translational Neurodevelopment and Department of Forensic and Neurodevelopmental Sciences, King's College London, Institute of Psychiatry, Psychology & Neuroscience, London, UK.
  • Canyelles JM; Behavioural and Developmental Psychiatry Clinical Academic Group, Behavioural Genetics Clinic, Adult Autism and ADHD Service, South London and Maudsley Foundation NHS Trust, London, UK.
  • Gothelf D; Developmental Imaging and Psychopathology Lab, Department of Psychiatry, School of Medicine, University of Geneva, Geneva, Switzerland.
  • Eliez S; Child and Adolescence Neuropsychiatry Unit, Department of Neuroscience, Children Hospital Bambino Gesù, Rome, Italy.
  • Breetvelt EJ; Child and Adolescence Neuropsychiatry Unit, Department of Neuroscience, Children Hospital Bambino Gesù, Rome, Italy.
  • Arango C; Hospital Universitario Fundacion Alcorcon, Alcorcon, Espana.
  • Vorstman JAS; Child and Adolescent Psychiatry Unit Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Sagol School of Neuroscience and Sackler School of Medicine Tel Aviv University, Tel Aviv, Israel.
Am J Med Genet A ; 176(10): 2182-2191, 2018 10.
Article em En | MEDLINE | ID: mdl-30194907
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Síndrome de DiGeorge / Transtornos Mentais Tipo de estudo: Diagnostic_studies / Risk_factors_studies Limite: Adolescent / Child / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Síndrome de DiGeorge / Transtornos Mentais Tipo de estudo: Diagnostic_studies / Risk_factors_studies Limite: Adolescent / Child / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article