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Translocation (13;22) in a hemangiopericytoma
Cancer Genetics and Cytogenetics
|April 15, 1986
Summary
A rare chromosomal abnormality, t(13;22)(q22;q11), was identified in a primary hemangiopericytoma. This finding may link to chromosome 22 changes seen in other cancers.
Area of Science:
- Cytogenetics
- Oncology
- Tumor Biology
Background:
- Hemangiopericytoma is a rare tumor.
- Cytogenetic abnormalities are implicated in tumorigenesis.