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.
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© 1982 S. Karger AG, Basel
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