The Pathology of Sickle Cell Haemoglobin C Disease and Sickle Cell Anaemia

Author:

Edington G. M.

Publisher

BMJ

Subject

General Medicine,Pathology and Forensic Medicine

Reference6 articles.

1. Edington, G. M. (1955). Trans. roy. Soc. trop. Med. Hyg., 49, 253-

2. Edington, G. M. (1956). W. Afr. Med. J. (New Series), 5, 71.

3. Trans. roy;Edington, G.M.; Lehmann, H.;Soc. trop. Med. Hvg; Lancet, 2, 173,1954

4. Itano, H. A., and Neel, J. V. (1950). Proc. nat. Acad. Sci. (Wash.), 36, 613.

5. Lambotte-Legrand, J., and Lambotte-Legrand, C. (1951). Ann. Soc.

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1. An octogenarian with hemoglobin S-C disease;American Journal of Hematology;1993-08

2. Vascular occlusion and infarction in sickle cell crisis and the sickle chest syndrome.;Journal of Clinical Pathology;1985-06-01

3. Neurological Complications of Hemoglobin SC Disease;Archives of Neurology;1984-03-01

4. The diagnosis of pulmonary thromboembolism in sickle cell disease;American Journal of Hematology;1979-11

5. Death Patterns in Sickle Cell Anemia;JAMA: The Journal of the American Medical Association;1975-08-25

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