REFERENCES
- Levine, P., Robinson, E., Stroup, M., McGee, R. and Bushnell, L. N.: A summary of atypical antibodies, rare genotypes and ABO hemolytic disease encountered in a one-year survey. Blood 11:1097–1117, 1956.
- Mollison, P. L.: Blood Transfusion in Clinical Medicine. Ed. 3. Oxford, England, Blackwell, 1958, p. 324.
- Nappi, R.: Eritroblastosi fetale da isosensibilizzazione verso il fattore rh”. Arch ostet. e ginec. 64: 402–405, 1959.
- Ebaugh, F. G., Jr., Emerson, F. D. and Ross, J. F.: Use of radioactive chromium51 as an erythrocyte tagging agent for the determination of red cell survival in vivo. J. Clin. Invest. 32:1260, 1953.
- Van Loghem, J. J., Bakx, C. J. A. and Klomp-Macnee, W.: Haemolytic disease of the newborn due to iso-immunization by the antigens c and Cw. Vox sang, (o.s.) 3:130–132, 1953.
- Hyatt, H. W., Sr.: Hemolytic disease of the newborn in a pair of monozygotic twins due to sensitization to blood factor hr'. Exper. Med. & Surg. 17:262–271, 1959.
- Race, R. R. and Sanger, R.: Blood Groups in Man. Ed. 3. Oxford, England, Blackwell, 1959, p. 132.
- Krivit, W.: The use of radioactive chromium in hemolytic anemias. Thesis, University of Minnesota Graduate School, Minneapolis, 1958.