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D R Higgs

Showing results (81-90 of 183) with videos related to

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British Journal of Haematology|August 1, 1987
Characterization of a new alpha zero thalassaemia defect in the South African populationS Vandenplas, D R Higgs, R D Nicholls, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 11, 2001
Identification of a conserved erythroid specific domain of histone acetylation across the alpha-globin gene clusterE Anguita, C A Johnson, W G Wood, et al.
Lancet (London, England)|March 7, 1981
Molecular basis for mild forms of homozygous beta-thalassaemiaD J Weatherall, L Pressley, W G Wood, et al.
Clinical and Laboratory Haematology|November 26, 2005
Phenotype/genotype relationships in sickle cell disease: a pilot twin studyM W Weatherall, D R Higgs, H Weiss, et al.
Nature|August 30, 1990
A truncated human chromosome 16 associated with alpha thalassaemia is stabilized by addition of telomeric repeat (TTAGGG)nA O Wilkie, J Lamb, P C Harris, et al.
Gene|June 22, 2001
The human GPI1 gene is required for efficient glycosylphosphatidylinositol biosynthesisA Tiede, R J Daniels, D R Higgs, 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.
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.
Pageof 19

Showing results (81-90 of 183) with videos related to

Sort By:
Pageof 19
British Journal of Haematology|August 1, 1987
Characterization of a new alpha zero thalassaemia defect in the South African populationS Vandenplas, D R Higgs, R D Nicholls, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 11, 2001
Identification of a conserved erythroid specific domain of histone acetylation across the alpha-globin gene clusterE Anguita, C A Johnson, W G Wood, et al.
Lancet (London, England)|March 7, 1981
Molecular basis for mild forms of homozygous beta-thalassaemiaD J Weatherall, L Pressley, W G Wood, et al.
Clinical and Laboratory Haematology|November 26, 2005
Phenotype/genotype relationships in sickle cell disease: a pilot twin studyM W Weatherall, D R Higgs, H Weiss, et al.
Nature|August 30, 1990
A truncated human chromosome 16 associated with alpha thalassaemia is stabilized by addition of telomeric repeat (TTAGGG)nA O Wilkie, J Lamb, P C Harris, et al.
Gene|June 22, 2001
The human GPI1 gene is required for efficient glycosylphosphatidylinositol biosynthesisA Tiede, R J Daniels, D R Higgs, 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.
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.
Pageof 19