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Acta Paediatrica (Oslo, Norway : 1992). Supplement|May 18, 2005
Substrate reduction therapy for lysosomal storage diseasesT M CoxMolecular Pharmacology|April 3, 2020
A Concise Review of Concepts in Opioid Pharmacology up to the Discovery of Endogenous OpioidsBrian M CoxJournal 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|May 1, 1980
Determination of alpha thalassaemia phenotypes by messenger RNA analysisD M Hunt, D R Higgs, J B Clegg, et al.Nucleic Acids Research|September 25, 1984
Independent recombination events between the duplicated human alpha globin genes; implications for their concerted evolutionD R Higgs, A V Hill, D K Bowden, 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.Pageof 257