The Thalassaemia Syndromes
- 1 January 1967
- journal article
- research article
- Published by S. Karger AG in Acta Haematologica
- Vol. 37 (4) , 181-188
- https://doi.org/10.1159/000209068
Abstract
Despite the similarity of clinical pictures, genetic patterns and the results of hemoglobin analyses in 2 patients, the type of anemia was entirely different: it was normocytic in 1 case and hypochromic microcytic in the other. The possible genetic explanations for the occurrence of different types of anemia in sickle cell-beta thalassemia disease are discussed.Keywords
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