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A heritable form of SMARCE1-related meningiomas with important implications for follow-up and family screening.
Gerkes, E H; Fock, J M; den Dunnen, W F A; van Belzen, M J; van der Lans, C A; Hoving, E W; Fakkert, I E; Smith, M J; Evans, D G; Olderode-Berends, M J W.
Afiliação
  • Gerkes EH; Department of Genetics, University of Groningen, University Medical Center Groningen, P.O. Box 30001, 9700 RB, Groningen, The Netherlands. e.h.gerkes@umcg.nl.
  • Fock JM; Department of Neurology, Child neurology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • den Dunnen WF; Department of Pathology and Medical Biology, Pathology division, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • van Belzen MJ; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • van der Lans CA; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Hoving EW; Department of Neurosurgery, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • Fakkert IE; Department of Genetics, University of Groningen, University Medical Center Groningen, P.O. Box 30001, 9700 RB, Groningen, The Netherlands.
  • Smith MJ; Manchester Centre for Genomic Medicine, Institute of Human Development, Manchester Academic Health Sciences Centre (MAHSC), St. Mary's Hospital, University of Manchester, Manchester, UK.
  • Evans DG; Manchester Centre for Genomic Medicine, Institute of Human Development, Manchester Academic Health Sciences Centre (MAHSC), St. Mary's Hospital, University of Manchester, Manchester, UK.
  • Olderode-Berends MJ; Department of Genetics, University of Groningen, University Medical Center Groningen, P.O. Box 30001, 9700 RB, Groningen, The Netherlands.
Neurogenetics ; 17(2): 83-9, 2016 Apr.
Article em En | MEDLINE | ID: mdl-26803492

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Neoplásicas Hereditárias / Proteínas Cromossômicas não Histona / Proteínas de Ligação a DNA / Meningioma Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Limite: Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Neoplásicas Hereditárias / Proteínas Cromossômicas não Histona / Proteínas de Ligação a DNA / Meningioma Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Limite: Adult / Child / Female / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article