Dyserythropoiesis in homozygous haemoglobin C disease
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2257.1982.tb00481.x/fullpdf
Reference10 articles.
1. Pathogenesis of hemolytic anemia in homozygous hemoglobin C disease;CHARACHE;J. clin. Invest.,1967
2. Some aspects of the pathophysiology of homozygous HbCC erythrocytes;FABRY;J. clin. Invest.,1981
3. Ultrastructural studies of the bone marrow in sickle cell anaemia. II. The morphology of erythropoietic cells and their response to deoxygenation in vitro;GRASSO;Br. J. Haemat.,1975
4. Allelomorphism and the chemical differences of the human haemoglobins A, S and C;HUNT;Nature (Lond.),1958
5. Molecular mechanism of hemolytic anemia in homozygous hemoglobin C disease. Electron microscopic study by the freeze-etching technique;LESSIN;J. exp. Med.,1969
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3. Ultrastructural abnormalities and arrest of protein biosynthesis in some erythroblasts from homozygotes for haemoglobin C and double heterozygotes for haemoglobin C and β-thalassaemia;Clinical & Laboratory Haematology;2008-06-28
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5. Congenital dyserythropoietic anaemias: clinical features, haematological morphology and new biochemical data;Blood Reviews;1998-09
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