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American Journal of Hematology
|
September 1, 1989
Hb Warsaw (beta 42 Phe----Val): an unstable hemoglobin with decreased oxygen affinity. I. Hematologic and clinical expression
G R Honig, M C Telfer, B B Rosenblum, et al.
American Journal of Hematology
|
January 1, 1978
Unbalanced globin chain synthesis by Hb Lincoln Park (anti-Lepore) reticulocytes
G R Honig, R G Mason, L M Tremaine, et al.
American Journal of Hematology
|
January 1, 1979
Three new variants of glucose-6-phosphate dehydrogenase associated with chronic nonspherocytic hemolytic anemia: G-6-PD Lincoln Park, G-6-PD Arlington Heights, and G-6-PD West Town
G R Honig, E Habacon, L N Vida, et al.
Pediatric Research
|
October 1, 1979
Sickle cell syndromes. III. Silent-carrier alpha-thalassemia in combination with hemoglobin S and hemoglobin C
G R Honig, R G Mason, L M Tremaine, et al.
Archives of Biochemistry and Biophysics
|
October 1, 1973
Hemoglobin heterogeneity in the rabbit: beta-112 isoleucine leads to valine
M Shamsuddin, R G Mason, C Cohen, et al.
Scandinavian Journal of Haematology
|
May 1, 1983
Acetylesterase in lymphoblastic leukaemia associated with thymic enlargement
R D Barr, M Koekebakker, F Cameron, et al.
Blood
|
April 1, 1981
Hemoglobin Petah Tikva (alpha 110 ala replaced by asp): a new unstable variant with alpha-thalassemia-like expression
G R Honig, M Shamsuddin, R Zaizov, et al.
Pediatric Research
|
June 1, 1976
Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia
G R Honig, U Gunay, R G Mason, et al.
American Journal of Diseases of Children (1960)
|
December 1, 1973
Commercial preparations of prothrombin complex. A clinical comparison
U Gunay, H S Choi, H S Maurer, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1974
Sites of acetylation of sickle cell hemoglobin by aspirin
M Shamsuddin, R G Mason, J M Ritchey, et al.
Page
of 8
Search research articles
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Showing results (41-50 of 73) with videos related to
Sort By:
Page
of 8
American Journal of Hematology
|
September 1, 1989
Hb Warsaw (beta 42 Phe----Val): an unstable hemoglobin with decreased oxygen affinity. I. Hematologic and clinical expression
G R Honig, M C Telfer, B B Rosenblum, et al.
American Journal of Hematology
|
January 1, 1978
Unbalanced globin chain synthesis by Hb Lincoln Park (anti-Lepore) reticulocytes
G R Honig, R G Mason, L M Tremaine, et al.
American Journal of Hematology
|
January 1, 1979
Three new variants of glucose-6-phosphate dehydrogenase associated with chronic nonspherocytic hemolytic anemia: G-6-PD Lincoln Park, G-6-PD Arlington Heights, and G-6-PD West Town
G R Honig, E Habacon, L N Vida, et al.
Pediatric Research
|
October 1, 1979
Sickle cell syndromes. III. Silent-carrier alpha-thalassemia in combination with hemoglobin S and hemoglobin C
G R Honig, R G Mason, L M Tremaine, et al.
Archives of Biochemistry and Biophysics
|
October 1, 1973
Hemoglobin heterogeneity in the rabbit: beta-112 isoleucine leads to valine
M Shamsuddin, R G Mason, C Cohen, et al.
Scandinavian Journal of Haematology
|
May 1, 1983
Acetylesterase in lymphoblastic leukaemia associated with thymic enlargement
R D Barr, M Koekebakker, F Cameron, et al.
Blood
|
April 1, 1981
Hemoglobin Petah Tikva (alpha 110 ala replaced by asp): a new unstable variant with alpha-thalassemia-like expression
G R Honig, M Shamsuddin, R Zaizov, et al.
Pediatric Research
|
June 1, 1976
Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia
G R Honig, U Gunay, R G Mason, et al.
American Journal of Diseases of Children (1960)
|
December 1, 1973
Commercial preparations of prothrombin complex. A clinical comparison
U Gunay, H S Choi, H S Maurer, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1974
Sites of acetylation of sickle cell hemoglobin by aspirin
M Shamsuddin, R G Mason, J M Ritchey, et al.
Page
of 8