Cytogenetic and loss of heterozygosity studies in ependymomas, pilocytic astrocytomas, and oligodendrogliomas

Cytogenetic and/or loss of heterozygosity studies were performed on 13 ependymomas, 11 pilocytic astrocytomas, and 18 oligodendrogliomas. Loss of chromosome 22 was the most frequent genetic abnormality among the ependymomas. We found no consistent genetic abnormality in pilocytic astrocytomas. The m...

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Veröffentlicht in:	Genes chromosomes & cancer 1992-11, Vol.5 (4), p.348-356
Hauptverfasser:	Ransom, David T., Ritland, Steve R., Kimmel, David W., Moertel, Cheryl A., Dahl, Richard J., Scheithauer, Bernd W., Kelly, Patrick J., Jenkins, Robert B.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Aged Alleles astrocytoma Astrocytoma - blood Astrocytoma - genetics Astrocytoma - pathology Brain Neoplasms - blood Brain Neoplasms - genetics Brain Neoplasms - pathology Child Child, Preschool chromosome 11 chromosome 22 chromosome 9 Chromosome Aberrations Chromosomes, Human, Pair 19 - ultrastructure cytogenetics DNA, Neoplasm - blood DNA, Neoplasm - genetics ependymoma Ependymoma - blood Ependymoma - genetics Ependymoma - pathology Female Genetic Markers Humans Infant Karyotyping Male man Middle Aged oligodendroglioma Oligodendroglioma - blood Oligodendroglioma - genetics Oligodendroglioma - pathology Sequence Deletion
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