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Examination of the genetic factors underlying the cognitive variability associated with neurofibromatosis type 1.
Ottenhoff, Myrthe J; Rietman, André B; Mous, Sabine E; Plasschaert, Ellen; Gawehns, Daniela; Brems, Hilde; Oostenbrink, Rianne; van Minkelen, Rick; Nellist, Mark; Schorry, Elizabeth; Legius, Eric; Moll, Henriette A; Elgersma, Ype.
Afiliação
  • Ottenhoff MJ; Department of Neuroscience, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Rietman AB; Department of Pediatrics, Erasmus Medical Center-Sophia Children's Hospital, Rotterdam, The Netherlands.
  • Mous SE; The ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Plasschaert E; The ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Gawehns D; Department of Child and Adolescent Psychiatry and Psychology, Erasmus Medical Center-Sophia Children's Hospital, Rotterdam, The Netherlands.
  • Brems H; The ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Oostenbrink R; Department of Child and Adolescent Psychiatry and Psychology, Erasmus Medical Center-Sophia Children's Hospital, Rotterdam, The Netherlands.
  • van Minkelen R; The ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Nellist M; Department of Child and Adolescent Psychiatry and Psychology, Erasmus Medical Center-Sophia Children's Hospital, Rotterdam, The Netherlands.
  • Schorry E; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Legius E; Department of Pediatrics, Erasmus Medical Center-Sophia Children's Hospital, Rotterdam, The Netherlands.
  • Moll HA; The ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus Medical Center, Rotterdam, The Netherlands.
Genet Med ; 22(5): 889-897, 2020 05.
Article em En | MEDLINE | ID: mdl-32015538
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neurofibromatose 1 Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Child / Humans Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Holanda
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neurofibromatose 1 Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Child / Humans Idioma: En Revista: Genet Med Assunto da revista: GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Holanda