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Proceedings of the National Academy of Sciences of the United States of America|June 1, 1980
Gene deletions in alpha thalassemia prove that the 5' zeta locus is functionalL Pressley, D R Higgs, J B Clegg, et al.Lancet (London, England)|August 20, 1977
Pattern of maternal F-cell production during pregnancyN Popat, W G Wood, D J Weatherall, et al.Clinical and Laboratory Haematology|January 1, 1981
Ultrastructure of red cells containing haemoglobin H inclusions induced by redox dyesS N Wickramasinghe, M Hughes, D R Higgs, et al.The American Journal of Medicine|August 1, 1983
Clinical features and molecular analysis of acquired hemoglobin H diseaseD R Higgs, W G Wood, C Barton, et al.Ciba Foundation Symposium|June 27, 1979
Human haemoglobin geneticsD J Weatherall, J B Clegg, W G Wood, et al.Journal of Clinical Pathology|June 1, 1985
Vascular occlusion and infarction in sickle cell crisis and the sickle chest syndromeN A Athanasou, C Hatton, J O McGee, et al.British Journal of Haematology|October 1, 1988
The molecular basis of thalassaemia major and thalassaemia intermedia in Asian Indians: application to prenatal diagnosisS L Thein, C Hesketh, R B Wallace, et al.Nature|December 4, 1980
Defective synthesis of HbE is due to reduced levels of beta E mRNAJ Traeger, W G Wood, J B Clegg, et al.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.Pageof 28