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Chromosomes in the genesis and progression of ependymomas.
Rogatto, S R; Casartelli, C; Rainho, C A; Barbieri-Neto, J.
Afiliación
  • Rogatto SR; Departamento de Biologia Geral, CCB, Universidade Estadual de Londrina, Brazil.
Cancer Genet Cytogenet ; 69(2): 146-52, 1993 Sep.
Article en En | MEDLINE | ID: mdl-8402555
Cytogenetic analysis was performed on cultures of primary ependymal tumors with different degrees of malignancy (I-IV) obtained from four patients, none of whom had received therapy before karyotypic evaluation. The most common abnormalities were monosomy 17 and 22 in four cases and losses of sex chromosomes in three cases. Structural rearrangements of chromosome 2 were a finding for all cases and involved loss of material at 2q32-34. Other structural chromosome abnormalities detected involved chromosomes 4, 6, 10, 11, 12, and X. We also reviewed data on 22 cases previously reported.
Asunto(s)
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Bases de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Aberraciones Cromosómicas / Ependimoma Límite: Humans Idioma: En Revista: Cancer Genet Cytogenet Año: 1993 Tipo del documento: Article País de afiliación: Brasil
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Bases de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Aberraciones Cromosómicas / Ependimoma Límite: Humans Idioma: En Revista: Cancer Genet Cytogenet Año: 1993 Tipo del documento: Article País de afiliación: Brasil