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British 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 WeatherallThe American Journal of Tropical Medicine and Hygiene|May 27, 1999
Reduced soluble transferrin receptor concentrations in acute malaria in VanuatuT N Williams, K Maitland, D C Rees, et al.Lancet (London, England)|September 25, 1976
A model for the persistence or reactivation of fetal haemoglobin productionD J Weatherall, J B Clegg, W G WoodJournal of Medical Genetics|June 1, 1975
Homozygous beta thalassaemia in LiberiaM C Willcox, D J Weatherall, J B CleggLancet (London, England)|October 28, 1995
World distribution of factor V LeidenD C Rees, M Cox, J B CleggBritish Journal of Haematology|April 1, 1976
Assay of thalassaemic messenger RNA in the wheat germ systemJ Pritchard, J Longley, J B Clegg, et al.Acta Haematologica|January 1, 1987
Alpha-thalassaemia and the malaria hypothesisA V Hill, J Flint, D J Weatherall, et al.Journal of Medical Genetics|June 1, 1977
Mild sickle-cell anaemia in Iran associated with high levels of fetal haemoglobinM Haghshenass, F Ismail-Beigi, J B Clegg, et al.Pageof 45