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Lancet (London, England)|September 25, 1976
A model for the persistence or reactivation of fetal haemoglobin productionD J Weatherall, J B Clegg, W G WoodTransactions of the Royal Society of Tropical Medicine and Hygiene|January 1, 1984
The deoxyuridine suppression test in severe anaemia following Plasmodium falciparum malariaS H Abdalla, S N Wickramasinghe, D J WeatherallCurrent Topics in Microbiology and Immunology|November 4, 2005
The clinical and pathophysiological features of malarial anaemiaD J Roberts, C Casals-Pascual, D J WeatherallClinical Science and Molecular Medicine|January 1, 1978
Intensive iron-chelation therapy with desferrioxamine in iron-loading anaemiasM J Pippard, S T Callender, D J WeatherallBritish Journal of Haematology|March 18, 2008
Is the beta thalassaemia trait of clinical importance?A Premawardhena, M Arambepola, N Katugaha, et al.Journal of Medical Genetics|June 1, 1975
Homozygous beta thalassaemia in LiberiaM C Willcox, D J Weatherall, J B CleggBritish Journal of Haematology|December 1, 1991
Rare beta-thalassaemia mutations in Asian indiansN Y Varawalla, J M Old, D J WeatherallBlood|December 1, 1986
The British form of hereditary persistence of fetal hemoglobin results from a single base mutation adjacent to an S1 hypersensitive site 5' to the A gamma globin geneV E Tate, W G Wood, D J WeatherallLancet (London, England)|October 6, 1990
Rapid detection and prenatal diagnosis of beta-thalassaemia: studies in Indian and Cypriot populations in the UKJ M Old, N Y Varawalla, D J WeatherallMedicine|November 1, 1990
A chronic granulomatous syndrome of unknown originJ S Friedland, D J Weatherall, J G LedinghamPageof 27