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Lancet (London, England)|June 2, 1979
Cellular origins of the fetal-haemoglobin-containing cells of normal adultsC Bunch, W G Wood, D J Weatherall, et al.Blood|June 1, 1985
Alpha zero-thalassemia due to recombination between the alpha 1-globin gene and an AluI repeatR D Nicholls, D R Higgs, J B Clegg, et al.Progress in Clinical and Biological Research|January 1, 1989
The spectrum of beta-thalassaemia in BurmaJ M Brown, S L Thein, K M Mar, et al.Proceedings of the National Academy of Sciences of the United States of America|August 1, 1983
Molecular basis of length polymorphism in the human zeta-globin gene complexS E Goodbourn, D R Higgs, J B Clegg, et al.Lancet (London, England)|June 4, 1983
The molecular basis for the clinical diversity of beta thalassaemia in CypriotsJ S Wainscoat, J M Old, D J Weatherall, et al.Proceedings of the National Academy of Sciences of the United States of America|May 1, 1979
Partial deletion of beta-globin gene DNA in certain patients with beta 0-thalassemiaS H Orkin, J M Old, D J Weatherall, et al.Journal of Medical Genetics|June 1, 1987
High frequency of beta thalassaemia in a small island population in MelanesiaD K Bowden, A V Hill, D J Weatherall, et al.Journal of Medical Genetics|August 1, 1979
G gamma beta + type of hereditary persistence of fetal haemoglobin in association with Hb CD R Higgs, J B Clegg, W G Wood, et al.Lancet (London, England)|October 8, 1977
Iron absorption in iron-loading anaemias: Effect of subcutaneous desferrioxamine infusionsM J Pippard, S T Callender, G T Warner, et al.Blood|November 11, 1999
Why are hemoglobin F levels increased in HbE/beta thalassemia?D C Rees, J B Porter, J B Clegg, et al.Pageof 27