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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.
British Journal of Haematology|November 1, 1982
The molecular basis for beta o thalassaemia intermedia in an Iranian individualR J Trent, J S Wainscoat, E R Huehns, et al.
Human Genetics|June 1, 1989
The frequency and origin of the sickle cell mutation in the district of Coruche/PortugalC Monteiro, J Rueff, A B Falcao, et al.
The EMBO Journal|August 1, 1986
Molecular characterisation of a hypervariable region downstream of the human alpha-globin gene clusterA P Jarman, R D Nicholls, D J Weatherall, et al.
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