Trisomy 8 detection in granulomonocytic, erythrocytic and megakaryocytic lineages by chromosomal in situ suppression hybridization in a case of refractory anaemia with ringed sideroblasts complicating the course of paroxysmal nocturnal haemoglobinuria
- 1 June 1992
- journal article
- Published by Wiley in British Journal of Haematology
- Vol. 81 (2) , 296-304
- https://doi.org/10.1111/j.1365-2141.1992.tb08223.x
Abstract
No abstract availableKeywords
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