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Parental perspectives on Phelan-McDermid syndrome: Results of a worldwide survey.
Landlust, Annemiek M; Koza, Sylvia A; Carbin, Maya; Walinga, Margreet; Robert, Sandra; Cooke, Jennifer; Vyshka, Klea; van Balkom, Ingrid D C; van Ravenswaaij-Arts, Conny.
Afiliação
  • Landlust AM; Autism Team Northern-Netherlands, Jonx, Department of (Youth) Mental Health and Autism, Lentis Psychiatric Institute, Groningen, the Netherlands; University of Groningen, University Medical Centre Groningen, Department of Genetics, Groningen, the Netherlands. Electronic address: a.landlust@lentis.nl
  • Koza SA; University of Groningen, University Medical Centre Groningen, Department of Genetics, Groningen, the Netherlands.
  • Carbin M; Phelan-McDermid Association, the Netherlands.
  • Walinga M; University of Groningen, University Medical Centre Groningen, Department of Genetics, Groningen, the Netherlands.
  • Robert S; (Swiss Representative of) Phelan-McDermid-Gesellschaft e.V. Geschäftsstelle Universitätsklinikum Ulm, Sekretariat Neurologie, Ulm, Germany.
  • Cooke J; Forensic and Neurodevelopmental Sciences Department, Institute of Psychiatry, Psychology, and Neuroscience, King's College London, United Kingdom.
  • Vyshka K; ERN ITHACA Guideline Working Group, ERN ITHACA Project Management & Legal Office, Clinical Genetics Department, Robert Debré University Hospital, Paris, France.
  • van Balkom IDC; Autism Team Northern-Netherlands, Jonx, Department of (Youth) Mental Health and Autism, Lentis Psychiatric Institute, Groningen, the Netherlands; Rob Giel Research Centre, Department of Psychiatry, University Medical Center Groningen, Groningen, the Netherlands.
  • van Ravenswaaij-Arts C; Autism Team Northern-Netherlands, Jonx, Department of (Youth) Mental Health and Autism, Lentis Psychiatric Institute, Groningen, the Netherlands; University of Groningen, University Medical Centre Groningen, Department of Genetics, Groningen, the Netherlands.
Eur J Med Genet ; 66(7): 104771, 2023 Jul.
Article em En | MEDLINE | ID: mdl-37120079
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Cromossômicos / Deficiência Intelectual Tipo de estudo: Guideline / Qualitative_research / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos Cromossômicos / Deficiência Intelectual Tipo de estudo: Guideline / Qualitative_research / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article