A Complex Ph1Translocation in a Patient with Primary Thrombocythaemia
- 1 April 1981
- journal article
- research article
- Published by Wiley in British Journal of Haematology
- Vol. 47 (4) , 571-575
- https://doi.org/10.1111/j.1365-2141.1981.tb02686.x
Abstract
Routine blood examination of a 27 yr old [human] female revealed a platelet count of 2000 .times. 109[cells]/l. Bone marrow cells showed the Philadelphia chromosome which was 1 product of a complex rearrangement of chromosomes 9, 22 and X. Her platelet count was lowered by plateletphoresis and chemotherapy [nitrogen mustard, busulphan]. She remains in good health 19 mo. later, but her thrombocythemia is considered to be an early manifestation of chronic myeloid leukemia.This publication has 11 references indexed in Scilit:
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