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Cell|February 1, 1979
Deficient heme synthesis as the cause of noninducibility of hemoglobin synthesis in a Friend erythroleukemia cell lineT R Rutherford, D J WeatherallPhilosophical 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 CleggBritish Journal of Haematology|December 1, 1976
The Negro variety of hereditary persistence of fetal haemoglobin is a mild form of thalassaemiaS Charache, J B Clegg, D J WeatherallProceedings of the National Academy of Sciences of the United States of America|October 1, 1975
Imbalanced globin chain synthesis in heterozygous beta-thalassemic bone marrowG Chalevelakis, J B Clegg, D J WeatherallBritish Journal of Haematology|December 1, 1976
Globin synthesis in normal human bone marrowG Chalevelakis, J B Clegg, D J WeatherallLancet (London, England)|September 25, 1976
A model for the persistence or reactivation of fetal haemoglobin productionD J Weatherall, J B Clegg, W G WoodPageof 34