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J Dover

Showing results (11-20 of 128) with videos related to

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Progress in Clinical and Biological Research|January 1, 1989
Stimulation of fetal hemoglobin production by hydroxyurea in sickle cell anemiaG J Dover, S Charache
American Journal of Hematology|June 1, 1989
Frequency of congenital anomalies in patients with histiocytosis XC Sheils, G J Dover
Seminars in Oncology|June 1, 1992
Hydroxyurea induction of fetal hemoglobin synthesis in sickle-cell diseaseG J Dover, S Charache
Annals of the New York Academy of Sciences|January 1, 1989
Chemotherapy and hemoglobin F synthesis in sickle cell diseaseG J Dover, S Charache
The New England Journal of Medicine|September 1, 1994
Therapy for beta-thalassemia--a paradigm for the treatment of genetic disordersG J Dover, D Valle
Progress in Clinical and Biological Research|January 1, 1987
The effect of increased fetal hemoglobin production on the frequency of vaso-occlusive crisis in sickle cell diseaseG J Dover, S Charache
Progress in Clinical and Biological Research|January 1, 1987
Increasing fetal hemoglobin production in sickle cell disease: results of clinical trialsG J Dover, S Charache
Progress in Clinical and Biological Research|January 1, 1984
The effects of variable doses of 5-azacytidine on fetal hemoglobin production in sickle cell anemiaG J Dover, S H Charache
The Biological Bulletin|January 5, 2018
On the Mechanism of Oriented Myoblast Differentiation in an Applied Electric FieldColin D McCaig, Philippa J Dover
Archives of Disease in Childhood|May 23, 2007
How to diagnose autismClare J Dover, Ann Le Couteur
Pageof 13

Showing results (11-20 of 128) with videos related to

Sort By:
Pageof 13
Progress in Clinical and Biological Research|January 1, 1989
Stimulation of fetal hemoglobin production by hydroxyurea in sickle cell anemiaG J Dover, S Charache
American Journal of Hematology|June 1, 1989
Frequency of congenital anomalies in patients with histiocytosis XC Sheils, G J Dover
Seminars in Oncology|June 1, 1992
Hydroxyurea induction of fetal hemoglobin synthesis in sickle-cell diseaseG J Dover, S Charache
Annals of the New York Academy of Sciences|January 1, 1989
Chemotherapy and hemoglobin F synthesis in sickle cell diseaseG J Dover, S Charache
The New England Journal of Medicine|September 1, 1994
Therapy for beta-thalassemia--a paradigm for the treatment of genetic disordersG J Dover, D Valle
Progress in Clinical and Biological Research|January 1, 1987
The effect of increased fetal hemoglobin production on the frequency of vaso-occlusive crisis in sickle cell diseaseG J Dover, S Charache
Progress in Clinical and Biological Research|January 1, 1987
Increasing fetal hemoglobin production in sickle cell disease: results of clinical trialsG J Dover, S Charache
Progress in Clinical and Biological Research|January 1, 1984
The effects of variable doses of 5-azacytidine on fetal hemoglobin production in sickle cell anemiaG J Dover, S H Charache
The Biological Bulletin|January 5, 2018
On the Mechanism of Oriented Myoblast Differentiation in an Applied Electric FieldColin D McCaig, Philippa J Dover
Archives of Disease in Childhood|May 23, 2007
How to diagnose autismClare J Dover, Ann Le Couteur
Pageof 13