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Blood|September 10, 1998
Is hemoglobin instability important in the interaction between hemoglobin E and beta thalassemia?D C Rees, J B Clegg, D J WeatherallBlood|November 11, 1999
Why are hemoglobin F levels increased in HbE/beta thalassemia?D C Rees, J B Porter, J B Clegg, et al.Annals of the New York Academy of Sciences|July 21, 1998
The hemoglobin E syndromesD C Rees, L Styles, E P Vichinsky, et al.British Journal of Haematology|November 25, 1998
Alpha thalassaemia is associated with increased soluble transferrin receptor levelsD C Rees, T N Williams, K Maitland, et al.Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 7, 1975
The alpha-chain-termination mutants and their relation to the alpha-thalassaemiasD J Weatherall, J B CleggProceedings of the Association of American Physicians|July 27, 1999
Thalassemia and malaria: new insights into an old problemJ B Clegg, D J WeatherallGenes and Immunity|September 5, 2002
Genetic variability in response to infection: malaria and afterD J Weatherall, J B CleggBulletin of the World Health Organization|September 8, 2001
Inherited haemoglobin disorders: an increasing global health problemD J Weatherall, J B CleggBlood|October 1, 1996
Interaction of hemoglobin E and pyrimidine 5' nucleotidase deficiencyD C Rees, J Duley, H A Simmonds, et al.Pageof 45