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B G Forget

Showing results (31-40 of 192) with videos related to

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Annual Review of Medicine|January 1, 1975
ThalassemiaB G Forget, D G Nathan
Pathobiology Annual|January 1, 1980
Pathogenesis of the thalassemia syndromesE J Benz, B G Forget
Genomics|December 1, 1991
Genomic organization of the human erythropoietin receptor geneL A Penny, B G Forget
Hematology/Oncology Clinics of North America|June 1, 1991
Delta beta thalassemia and hereditary persistence of fetal hemoglobinJ A Bollekens, B G Forget
Blood|November 1, 1989
The breakpoint of a large deletion causing hereditary persistence of fetal hemoglobin occurs within an erythroid DNA domain remote from the beta-globin gene clusterE A Feingold, B G Forget
The Journal of Clinical Investigation|December 1, 1971
Defect in messenger RNA for human hemoglobin synthesis in beta thalassemiaE J Benz, B G Forget
Blood Cells, Molecules & Diseases|March 28, 1998
Hematologically important mutations: band 3 and protein 4.2 variants in hereditary spherocytosisP G Gallagher, B G Forget
Molecular and Cellular Biology|July 1, 1991
Negative regulation of globin gene expression during megakaryocytic differentiation of a human erythroleukemic cell lineN L Lumelsky, B G Forget
Blood Cells, Molecules & Diseases|January 1, 1996
Hematologically important mutations: spectrin variants in hereditary elliptocytosis and hereditary pyropoikilocytosisP G Gallagher, B G Forget
Seminars in Hematology|October 1, 1974
The biosynthesis of hemoglobinE J Benz, B G Forget
Pageof 20

Showing results (31-40 of 192) with videos related to

Sort By:
Pageof 20
Annual Review of Medicine|January 1, 1975
ThalassemiaB G Forget, D G Nathan
Pathobiology Annual|January 1, 1980
Pathogenesis of the thalassemia syndromesE J Benz, B G Forget
Genomics|December 1, 1991
Genomic organization of the human erythropoietin receptor geneL A Penny, B G Forget
Hematology/Oncology Clinics of North America|June 1, 1991
Delta beta thalassemia and hereditary persistence of fetal hemoglobinJ A Bollekens, B G Forget
Blood|November 1, 1989
The breakpoint of a large deletion causing hereditary persistence of fetal hemoglobin occurs within an erythroid DNA domain remote from the beta-globin gene clusterE A Feingold, B G Forget
The Journal of Clinical Investigation|December 1, 1971
Defect in messenger RNA for human hemoglobin synthesis in beta thalassemiaE J Benz, B G Forget
Blood Cells, Molecules & Diseases|March 28, 1998
Hematologically important mutations: band 3 and protein 4.2 variants in hereditary spherocytosisP G Gallagher, B G Forget
Molecular and Cellular Biology|July 1, 1991
Negative regulation of globin gene expression during megakaryocytic differentiation of a human erythroleukemic cell lineN L Lumelsky, B G Forget
Blood Cells, Molecules & Diseases|January 1, 1996
Hematologically important mutations: spectrin variants in hereditary elliptocytosis and hereditary pyropoikilocytosisP G Gallagher, B G Forget
Seminars in Hematology|October 1, 1974
The biosynthesis of hemoglobinE J Benz, B G Forget
Pageof 20