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Hemoglobin|January 1, 1987
Hb Mississippi [beta 44(CD3)Ser----Arg]: a new variant with anomalous propertiesJ G Adams, W T Morrison, R L Barlow, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1993
Sparing effect of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S at physiologic ligand saturationsW N Poillon, B C Kim, G P Rodgers, et al.
American Journal of Hematology|October 1, 1995
Filterability of mixtures of sickle and normal erythrocytesS Hasegawa, H Hiruma, N Uyesaka, et al.
Obstetrics and Gynecology|July 1, 1986
Management of factor XI deficiency in gynecologic and obstetric patientsM H Steinberg, S Saletan, M Funt, et al.
The New England Journal of Medicine|April 12, 1990
Hematologic responses of patients with sickle cell disease to treatment with hydroxyureaG P Rodgers, G J Dover, C T Noguchi, et al.
American Journal of Hematology|April 1, 1996
Disturbance of plasma and platelet thrombospondin levels in sickle cell diseaseP V Browne, D F Mosher, M H Steinberg, et al.
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