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Southern Medical Journal|December 1, 1985
Posttransfusion crises in sickle cell anemia: role of delayed hemolytic reactions to transfusionP F Milner, J E Squires, P J Larison, et al.American Journal of Hematology|January 1, 1976
Thalassemia intermedia caused by heterozygosity for both beta-thalassemia and hemoglobin Saki [beta 14 (A11) Leu replaced by Pro]P F Milner, C C Corley, W L Pomeroy, et al.Blood|January 1, 1984
Increased HbF in sickle cell anemia is determined by a factor linked to the beta S gene from one parentP F Milner, J D Leibfarth, J Ford, et al.Proceedings of the National Academy of Sciences of the United States of America|August 1, 1981
Direct identification of sickle cell anemia by blot hybridizationR F Geever, L B Wilson, F S Nallaseth, et al.American Journal of Hematology|April 1, 1986
The effect of Hb F and alpha-thalassemia on the red cell indices in sickle cell anemiaP F Milner, G J Garbutt, L V Nolan-Davis, et al.Journal of Medical Genetics|February 1, 1976
Linkage relationships between beta- and delta-structural loci and African forms of beta thalassaemiaD J Weatherall, J B Clegg, P F Milner, et al.Hemoglobin|January 1, 1977
Effect of 2, 3-diphosphoglycerate on the solubility of deoxy-sickle hemoglobinP H Swerdlow, R A Bryan, J F Bertles, et al.The Journal of Antimicrobial Chemotherapy|February 14, 2021
Treatment of methicillin-resistant Staphylococcus aureus (MRSA): updated guidelines from the UKNicholas M Brown, Erwin M Brown, The Journal of General Physiology|September 1, 1973
Light response of a giant Aplysia neuronA M Brown, H M BrownScience (New York, N.Y.)|November 17, 1972
Ionic basis of the photoresponse of Aplysia giant neuron: K + permeability increaseH M Brown, A M BrownPageof 1,162