Dover, George J.

Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia

Charache, S., Terrin, M. L., Moore, R. D., Dover, G. J., Barton, F. B., Eckert, S. V., McMahon, R. P., & Bonds, D. R. (1995) · New England Journal of Medicine

Hemoglobinopathies and Related DisordersBlood groups and transfusion

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Fetal hemoglobin in sickle cell anemia: determinants of response to hydroxyurea

Steinberg, M. H., Lu, Z.-H., Barton, F. B., Terrin, M. L., Charache, S., Dover, G. J., & Hydroxyurea, T. M. S. O. (1997) · Blood

Hemoglobinopathies and Related DisordersBlood groups and transfusion

Cited by 407

Fetal hemoglobin in sickle cell anemia: a glass half full?

Steinberg, M. H., Chui, D. H. K., Dover, G. J., Sebastiani, P., & Alsultan, A. (2014) · Blood

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 267

Individual variation in the production and survival of F cells in sickle-cell disease

Dover, G. J., Boyer, S. H., Charache, S., & Heintzelman, K. (1978) · New England Journal of Medicine

Hemoglobinopathies and Related DisordersHemoglobin structure and function

Cited by 144