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British Journal of Haematology|January 1, 1981
The genetics and molecular basis of alpha thalassaemia in association with Hb S in Jamaican NegroesD R Higgs, L Pressley, G R Serjeant, et al.The Johns Hopkins Medical Journal|June 1, 1980
alpha thalassemia in black populationsD R Higgs, L Pressley, J B Clegg, et al.British Journal of Haematology|November 1, 1981
Haemoglobin synthesis by fetal erythroid cells in an adult environmentC Bunch, W G Wood, D J Weatherall, et al.British Journal of Haematology|February 5, 1998
Beta-thalassaemia intermedia: is it possible consistently to predict phenotype from genotype?P J Ho, G W Hall, L Y Luo, et al.Journal of Medical Genetics|December 1, 1985
Prenatal diagnosis of the common haemoglobin disordersD J Weatherall, J M Old, S L Thein, et al.Lancet (London, England)|November 9, 1985
Relative roles of genetic factors, dietary deficiency, and infection in anaemia in Vanuatu, South-West PacificD K Bowden, A V Hill, D R Higgs, et al.British Journal of Haematology|August 1, 1984
Interaction of the alpha alpha alpha globin gene haplotype and sickle haemoglobinD R Higgs, J B Clegg, D J Weatherall, et al.British Journal of Haematology|July 1, 1980
Hb F synthesis in sickle cell anaemia: a comparison of Saudi Arab cases with those of African originW G Wood, M E Pembrey, G R Serjeant, et al.British Journal of Haematology|October 1, 1984
Characterization of an Indian (delta beta)0 thalassaemiaJ S Wainscoat, J M Old, W G Wood, et al.British Journal of Haematology|June 1, 1981
Haemoglobin synthesis in human erythroid bursts during ontogeny: reproducibility and sensitivity to culture conditionsP D Darbre, S M Lauckner, J W Adamson, et al.Pageof 27