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P F Milner

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American Journal of Clinical Pathology|July 1, 1981
The occurrence and identification of alpha-thalassemia-2 among hemoglobin S heterozygotesA E Felice, C A Altay, P F Milner, et al.
American Journal of Hematology|August 1, 1993
Direct demonstration that the A gamma T globin gene is linked to the 4 bp promoter deletion in the beta A chromosome of sickle cell traitsJ G Gilman, O Josifovska, S Erlingsson, et al.
Hemoglobin|January 1, 1979
Microchromatographic quantitation of fetal hemoglobin in patients with sickle cell diseaseE C Abraham, J Carver, J Döbler, et al.
The Journal of Reproductive Medicine|February 1, 1984
Sickle-cell-induced hematuria in pregnancy. The current diagnostic and therapeutic approachS H Kassam, H A Hadi, H E Fadel, et al.
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.
The New England Journal of Medicine|December 24, 1970
Hemoglobin O arab in four negro families and its interaction with hemoglobin S and hemoglobin CP F Milner, C Miller, R Grey, 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.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
American Journal of Clinical Pathology|July 1, 1981
The occurrence and identification of alpha-thalassemia-2 among hemoglobin S heterozygotesA E Felice, C A Altay, P F Milner, et al.
American Journal of Hematology|August 1, 1993
Direct demonstration that the A gamma T globin gene is linked to the 4 bp promoter deletion in the beta A chromosome of sickle cell traitsJ G Gilman, O Josifovska, S Erlingsson, et al.
Hemoglobin|January 1, 1979
Microchromatographic quantitation of fetal hemoglobin in patients with sickle cell diseaseE C Abraham, J Carver, J Döbler, et al.
The Journal of Reproductive Medicine|February 1, 1984
Sickle-cell-induced hematuria in pregnancy. The current diagnostic and therapeutic approachS H Kassam, H A Hadi, H E Fadel, et al.
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.
The New England Journal of Medicine|December 24, 1970
Hemoglobin O arab in four negro families and its interaction with hemoglobin S and hemoglobin CP F Milner, C Miller, R Grey, 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.
Pageof 5