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Progress in Clinical and Biological Research|January 1, 1981
The clinical effects of Hb S, an overviewP F MilnerThe Journal of Clinical Investigation|December 1, 1973
Life span of carbamylated red cells in sickle cell anemiaP F Milner, S CharacheBlood|December 1, 1982
Bone marrow infarction in sickle cell anemia: correlation with hematologic profilesP F Milner, M BrownProgress in Clinical and Biological Research|January 1, 1981
The unstable hemoglobins: a reviewP F Milner, R N WrightstoneBritish Journal of Haematology|October 1, 1976
Studies of the proporation and synthesis of haemoblogin C Philadelphia in red cells of heterozygotes, a homozygote, and a heterozygote for both haemoglobin G and alpha thalassaemiaP F Milner, T H HuismanAmerican Journal of Clinical Pathology|July 1, 1975
Rapid citrate-agar electrophoresis in routine screening for hemoglobinopathies using a simple hemolysateP F Milner, H M GoodenArchives of Otolaryngology (Chicago, Ill. : 1960)|September 1, 1982
Elective surgery in patients with sickle cell anemiaN J Coker, P F MilnerAmerican Journal of Hematology|June 1, 1996
Cardiovascular function during rest and exercise in patients with sickle-cell anemia and coexisting alpha thalassemia-2D S Braden, W Covitz, P F MilnerAmerican Journal of Obstetrics and Gynecology|October 1, 1980
Outcome of pregnancy in sickle cell anemia and sickle cell-hemoglobin C disease. An analysis of 181 pregnancies in 98 patients, and a review of the literatureP F Milner, B R Jones, J DöblerPageof 79