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R Higgs

Showing results (261-270 of 469) with videos related to

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British Journal of Haematology|November 1, 1980
The genetic basis of Hb Q-H diseaseD R Higgs, D M Hunt, H C Drysdale, et al.
International Journal of Laboratory Hematology|July 23, 2008
The changing face of homozygous sickle cell disease: 102 patients over 60 yearsG R Serjeant, B E Serjeant, K P Mason, et al.
The New England Journal of Medicine|December 11, 1980
A new genetic basis for hemoglobin-H diseaseL Pressley, D R Higgs, J B Clegg, et al.
Blood|January 1, 1987
The cellular basis for different fetal hemoglobin levels among sickle cell individuals with two, three, and four alpha-globin genesG J Dover, V T Chang, S H Boyer, et al.
The EMBO Journal|December 1, 1992
Analysis of the human alpha globin upstream regulatory element (HS-40) in transgenic miceJ A Sharpe, P S Chan-Thomas, J Lida, et al.
Nature|November 24, 1983
Alpha-thalassaemia caused by a polyadenylation signal mutationD R Higgs, S E Goodbourn, J Lamb, et al.
Haematologica|February 12, 2002
Clinical phenotypes and molecular characterization of Hb H-Paksé diseaseVip Viprakasit, Voravarn S Tanphaichitr, Parichat Pung-Amritt, et al.
Blood|February 1, 1988
The polyadenylation site mutation in the alpha-globin gene clusterS L Thein, R B Wallace, L Pressley, et al.
British Journal of Haematology|July 1, 1986
Alpha thalassaemia in an Italian populationC Velati, M Sampietro, M Biassoni, et al.
American Journal of Hematology|February 24, 2004
Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H diseaseVip Viprakasit, Voravarn S Tanphaichitr, Gavivann Veerakul, et al.
Pageof 47

Showing results (261-270 of 469) with videos related to

Sort By:
Pageof 47
British Journal of Haematology|November 1, 1980
The genetic basis of Hb Q-H diseaseD R Higgs, D M Hunt, H C Drysdale, et al.
International Journal of Laboratory Hematology|July 23, 2008
The changing face of homozygous sickle cell disease: 102 patients over 60 yearsG R Serjeant, B E Serjeant, K P Mason, et al.
The New England Journal of Medicine|December 11, 1980
A new genetic basis for hemoglobin-H diseaseL Pressley, D R Higgs, J B Clegg, et al.
Blood|January 1, 1987
The cellular basis for different fetal hemoglobin levels among sickle cell individuals with two, three, and four alpha-globin genesG J Dover, V T Chang, S H Boyer, et al.
The EMBO Journal|December 1, 1992
Analysis of the human alpha globin upstream regulatory element (HS-40) in transgenic miceJ A Sharpe, P S Chan-Thomas, J Lida, et al.
Nature|November 24, 1983
Alpha-thalassaemia caused by a polyadenylation signal mutationD R Higgs, S E Goodbourn, J Lamb, et al.
Haematologica|February 12, 2002
Clinical phenotypes and molecular characterization of Hb H-Paksé diseaseVip Viprakasit, Voravarn S Tanphaichitr, Parichat Pung-Amritt, et al.
Blood|February 1, 1988
The polyadenylation site mutation in the alpha-globin gene clusterS L Thein, R B Wallace, L Pressley, et al.
British Journal of Haematology|July 1, 1986
Alpha thalassaemia in an Italian populationC Velati, M Sampietro, M Biassoni, et al.
American Journal of Hematology|February 24, 2004
Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H diseaseVip Viprakasit, Voravarn S Tanphaichitr, Gavivann Veerakul, et al.
Pageof 47