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Autism in neurofibromatosis type 1: misuse of covariance to dismiss autistic trait burden.
Morris, Stephanie M; Acosta, Maria T; Garg, Shruti; Green, Jonathan; Legius, Eric; North, Kathryn; Payne, Jonathan M; Weiss, Lauren A; Constantino, John N; Gutmann, David H.
Afiliação
  • Morris SM; Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA.
  • Acosta MT; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
  • Garg S; Royal Manchester Children's Hospital, Manchester, UK.
  • Green J; Royal Manchester Children's Hospital, Manchester, UK.
  • Legius E; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • North K; Department of Pediatrics, Murdoch Children's Research Institute, University of Melbourne, Melbourne, Vic, Australia.
  • Payne JM; Department of Pediatrics, Murdoch Children's Research Institute, University of Melbourne, Melbourne, Vic, Australia.
  • Weiss LA; Department of Psychiatry, Institute for Human Genetics, University of California, San Francisco, CA, USA.
  • Constantino JN; Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA.
  • Gutmann DH; Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA.
Dev Med Child Neurol ; 63(2): 233-234, 2021 02.
Article em En | MEDLINE | ID: mdl-32815557
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtorno do Deficit de Atenção com Hiperatividade / Transtorno Autístico / Neurofibromatose 1 / Transtorno do Espectro Autista Tipo de estudo: Etiology_studies Limite: Child / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtorno do Deficit de Atenção com Hiperatividade / Transtorno Autístico / Neurofibromatose 1 / Transtorno do Espectro Autista Tipo de estudo: Etiology_studies Limite: Child / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article