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Synchronous gemistocytic astrocytoma IDH-mutant and oligodendroglioma IDH-mutant and 1p/19q-codeleted in a patient with CCDC26 polymorphism.
Vaubel, Rachael A; Kollmeyer, Thomas M; Caron, Alissa A; Barr Fritcher, Emily G; Voss, Jesse S; Liang, Haohai; Jenkins, Robert B; Giannini, Caterina; Kipp, Benjamin R.
Afiliação
  • Vaubel RA; Department of Anatomic Pathology, Mayo Clinic, Rochester, MN, USA.
  • Kollmeyer TM; Department of Experimental Pathology, Mayo Clinic, Rochester, MN, USA.
  • Caron AA; Department of Experimental Pathology, Mayo Clinic, Rochester, MN, USA.
  • Barr Fritcher EG; Department of Molecular Anatomic Pathology, Mayo Clinic, Rochester, MN, USA.
  • Voss JS; Department of Molecular Anatomic Pathology, Mayo Clinic, Rochester, MN, USA.
  • Liang H; Anatomic Pathology, WellStar Kennestone Hospital, Marietta, GA, USA.
  • Jenkins RB; Department of Experimental Pathology, Mayo Clinic, Rochester, MN, USA.
  • Giannini C; Department of Anatomic Pathology, Mayo Clinic, Rochester, MN, USA.
  • Kipp BR; Department of Anatomic Pathology, Mayo Clinic, Rochester, MN, USA. kipp.benjamin@mayo.edu.
Acta Neuropathol ; 134(2): 317-319, 2017 08.
Article em En | MEDLINE | ID: mdl-28550371
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 1 / Cromossomos Humanos Par 19 / Neoplasias Encefálicas / Deleção Cromossômica / Isocitrato Desidrogenase / Mutação Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 1 / Cromossomos Humanos Par 19 / Neoplasias Encefálicas / Deleção Cromossômica / Isocitrato Desidrogenase / Mutação Idioma: En Ano de publicação: 2017 Tipo de documento: Article