Clinical, hematological and genetic features of sickle-cell anemia and sickle cell-β thalassemia in a Brazilian population
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1980.tb01366.x/fullpdf
Reference21 articles.
1. Sickle-cell-thalassaemia disease in South Turkey;Aksoy;Brit. med. J.,1957
2. Historical note on the inheritance of sickle cell anemia;Azevedo;Amer. J. hum. Genet.,1973
3. Sickle cell anemia as a syndrome: a review of diagnostic features;Huisman;Amer. J. Hematol.,1979
4. A rapid whole blood solubility test to differentiate the sickle-cell trait from sickle-cell anemia;Huntsman;J. clin. Path.,1970
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2. The protective effect of the spleen in sickle cell patients. A comparative study between patients with asplenia/hyposplenism and hypersplenism;Frontiers in Physiology;2022-08-29
3. Echocardiografic abnormalities in patients with sickle cell/β-thalassemia do not depend on the β-thalassemia phenotype;Hematology, Transfusion and Cell Therapy;2019-04
4. A significant proportion of children of African descent with HbSβ 0 thalassaemia are inaccurately diagnosed based on phenotypic analyses alone;British Journal of Haematology;2018-05-24
5. Sickle cell/β-thalassemia: Comparison of Sβ0and Sβ+Brazilian patients followed at a single institution;Hematology;2016-05-28
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