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P. Mollison (1943)
The survival of transfused erythrocytes in haemolytic disease of the newborn*Archives of Disease in Childhood, 18
R. Brinkman, J. Jonxis (1935)
The occurrence of several kinds of hæmoglobin in human bloodThe Journal of Physiology, 85
F. Hall (1934)
A spectroscopic comparison of fœtal and maternal blood of the rabbit and goatThe Journal of Physiology, 82
R. Porter, F. Sanger (1948)
The free amino groups of haemoglobins.The Biochemical journal, 42 2
R. Darling, C. Smith, E. Asmussen, F. Cohen (1941)
SOME PROPERTIES OF HUMAN FETAL AND MATERNAL BLOOD.The Journal of clinical investigation, 20 6
Karl Singer, A. Chernoff (1952)
Studies on abnormal hemoglobins. III. The interrelationship of type S (sickle cell) hemoglobin and type F (alkali resistant) hemoglobin in sickle cell anemia.Blood, 7 1
Karl Singer, A. Chernoff, L. Singer (1951)
Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.Blood, 6 5
A. Chernoff, K. Singer (1952)
Studies on abnormal hemoglobins. IV. Persistence of fetal hemoglobin in the erythrocytes of normal children.Pediatrics, 9 4
G. Beaven, H. Hoch, E. Holiday (1951)
The haemoglobin of the human foetus and infant. Electrophoretic and spectroscopic differentiation of adult and foetal types.The Biochemical journal, 49 3
M. Andersch, Donald Wilson, M. Menten (1944)
SEDIMENTATION CONSTANTS AND ELECTROPHORETIC MOBILITIES OF ADULT AND FETAL CARBONYLHEMOGLOBINJournal of Biological Chemistry, 153
Karl Singer, B. Fisher (1951)
Studies on abnormal hemoglobins. V. The distribution of type S, sickle cell, hemoglobin and type F, alkali resistant, hemoglobin within the red cell population in sickle cell anemia.Blood, 7 12
J. Jonxis (1948)
Fœtal Hæmoglobin and ErythroblastosisNature, 161
R. Brinkman, J. Jonxis (1936)
Alkaline resistance and spreading velocity of fœtal and adult types of mammalian hæmoglobinThe Journal of Physiology, 88
K. Singer, A. Chernoff, L. Singer (1951)
Studies on abnormal hemoglobins. II. Their identification by means of the method of fractional denaturation.Blood, 6 5
F. Adams, S. Cunningham (1952)
Further studies on the blood of children with cyanotic heart disease with special reference to the hemoglobin.The Journal of pediatrics, 41 4
J. Barcroft (1933)
THE CONDITIONS OF FŒTAL RESPIRATIONThe Lancet, 222
IT HAS long been known that the period of fetal life is characterized by the synthesis of a distinct type of hemoglobin which is gradually, and finally completely, replaced by another type which is found in the blood of older infants, children, and adults. Differences between fetal and adult hemoglobin were first shown by von Korber1 in 1866 and von Krüger2 in 1887, both of whom demonstrated an increased resistance to alkali denaturation of the hemoglobin derived from fetal red cells. Many subsequent investigations have confirmed these observations, not only in humans, but also in many of the animal species as well.* In addition to differences in response to alkali denaturation, the two types of hemoglobin have been found to differ in oxygen and carbon dioxide affinity,f chemical structure,13 immunological properties ‡ crystalline configuration,16 and electrophoretic mobility.§ Most investigators have indicated that the differences lie in
American journal of diseases of children – American Medical Association
Published: Feb 1, 1954
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