On the nature of sickle-cell disease in the Arabian Peninsula
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00278681.pdf
Reference56 articles.
1. Ali, S. A.: Milder variant of sickle-cell disease in Arabs in Kuwait associated with unusually high level of foetal haemoglobin. Br. J. Haematol. 19, 613?623 (1970)
2. Beaven, G. H., Ellis, M. J., White, J. C.: Studies on human foetal haemoglobin. II. Foetal haemoglobin levels in healthy children and adults and in certain haematological disorders. Br. J. Haematol. 6, 201?222 (1960)
3. Bernstein, S. C., Bowman, J. E., Swift, H. H.: Modification of the acid technique for quantitation of foetal haemoglobin in individual erythrocytes. Hemoglobin 1, 313?331 (1977)
4. Bertles, J. F., Milner, M. F. A.: Irreversibly sickled erythrocytes: a consequence of the heterogeneous distribution of haemoglobin types in sickle-cell anaemia. J. Clin. Invest. 47, 1731?1741 (1968)
5. Bartles, J. F., Rabinovitz, R., Dobler, J.: Haemoglobin interaction: modification of solid phase composition in the sickling phenomenon. Science 169, 375?378 (1970)
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