Abstract
IN previous communications1,2 the existence of a third normal, embryonic hæmoglobin was reported to be present in the blood of fœtuses up to five months of intra-uterine life. The hæmolysates of the blood of these fœtuses were characterized by their electrophoretic mobility on filter paper in a buffer solution of p H 8.6, which was slower than that shown by the hæmolysates obtained from the cord blood of full-term new-borns. The paper electrophoresis method did not permit us, however, to separate the different hæmoglobin fractions present either in the fœtal or in the embryonic blood.
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References
Halbrecht, I., and Klibanaski, Ch., Nature, 178, 794 (1956).
Halbrecht, I., Klibanaski, Ch., Brzoza, H., and Lahav, M., Amer. J. Clin. Path., 29, 340 (1958).
Huisman, T. H. J., and Prins, H. K., Clin. Chim. Acta, 2, 307 (1957).
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HALBRECHT, I., KLIBANSKI, C. & ILAN, F. Co-existence of the Embryonic (Third Normal) Hæmoglobin Fraction with Erythroblastosis in the Blood of Two Full-term New-born Babies with Multiple Malformations. Nature 183, 327–328 (1959). https://doi.org/10.1038/183327a0
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DOI: https://doi.org/10.1038/183327a0
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