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Movement Disorder Phenotypes in Children With 22q11.2 Deletion Syndrome.
Cunningham, Adam C; Fung, Wilson; Massey, Thomas H; Hall, Jeremy; Owen, Michael J; van den Bree, Marianne B M; Peall, Kathryn J.
Afiliação
  • Cunningham AC; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK.
  • Fung W; Aneurin Bevan University Health Board, Royal Gwent Hospital, Newport, UK.
  • Massey TH; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK.
  • Hall J; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK.
  • Owen MJ; Neuroscience and Mental Health Research Institute, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK.
  • van den Bree MBM; MRC Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK.
  • Peall KJ; Neuroscience and Mental Health Research Institute, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, Cardiff, UK.
Mov Disord ; 35(7): 1272-1274, 2020 07.
Article em En | MEDLINE | ID: mdl-32379361
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Craniossinostoses / Síndrome de DiGeorge / Aracnodactilia / Transtornos dos Movimentos Limite: Child / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Craniossinostoses / Síndrome de DiGeorge / Aracnodactilia / Transtornos dos Movimentos Limite: Child / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article