Hemoglobin Interaction: Modification of Solid Phase Composition in the Sickling Phenomenon
Author:
Affiliation:
1. Hematology Unit, Medical Service, St. Luke's Hospital Center, and Department of Medicine, Columbia University College of Physicians and Surgeons, New York 10025
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference21 articles.
1. ALLISON, A.C., PROPERTIES OF SICKLE-CELL HAEMOGLOBIN, BIOCHEMICAL JOURNAL 65: 212 (1957).
2. BERTLES, J. F., BLOOD-THE JOURNAL OF HEMATOLOGY 33: 884 (1969).
3. BESSIS, M, REV HEMATOL 13: 249 (1958).
4. DOBLER, J, PHYSICAL STATE OF HEMOGLOBIN IN SICKLE-CELL ANEMIA ERTHROCYTES IN VIVO, JOURNAL OF EXPERIMENTAL MEDICINE 127: 711 (1968).
5. DOZY, A.M., STUDIES ON HETEROGENEITY OF HEMOGLOBIN .14. CHROMATOGRAPHY OF NORMAL AND ABNORMAL HUMAN HEMOGLOBIN TYPES ON CM-SEPHADEX, JOURNAL OF CHROMATOGRAPHY 40: 62 (1969).
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