Abstract
The internal and surface ultrastructural features of the white blood cells of a patient with hypergranular (M3) promyelocytic leukemia are described. Cytogenetical studies of the patient’s cells revealed the presence of two abnormal clones: The first, 45, XY, -7, and the second with an interstitial deletion in the long arm of chromosome 15 with break points at q22 and q26.
Original language | English |
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Pages (from-to) | 52-57 |
Number of pages | 6 |
Journal | Acta Haematologica |
Volume | 68 |
Issue number | 1 |
DOIs | |
State | Published - 1982 |
Keywords
- Cell ultrastructure
- Chromosomal translocation
- Electron microscopy
- Hypergranular (M) promyelocytic leukemia