Abstract
Blood consists of four components: erythrocytes, leukocytes, platelets, and plasma. Each blood component exhibits individual differences demonstrable by either immunologic or physico-chemical methods. These individual differences in the molecular structures of blood constituents are governed by genes or chromosomes and are generally known as allotypes, phenotypes, or simply types. Types which are genetically related have been assigned to the same system. The number of systems and specificities currently being used by some laboratories in paternity testing are listed in Table I.
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References
Race, R.R. and Sanger, R., Blood groups in man, ed. 1–5, F.A. Davis, Philadelphia, (1968).
Sussman, L.N., “Blood Grouping Tests. Medico-Legal Uses,” Charles C. Thomas, Springfield (1968).
Konugres, A.A. and Polesky, H.F., Use of blood groups in paternity testing, in “Paternity Testing,” Amer. Soc. Clin. Pathol., H.F. Polesky (ed), Chicago (1975), p. 1.
Schatkin, S.B., “Disputed Paternity Proceedings,” 4th Ed., M. Bender, New York (1967).
Polesky, H.F., “Paternity Testing,” Amer. Soc. Clin. Pathol, Chicago (1975).
Weiner, A.S., “Blood Groups and Transfusion,” 3rd ed., Charles C. Thomas, Springfield (1943).
Sussman, L.N., Titration and scoring in disputed parentage. Transfusion 5: 248 (1965).
Polesky, H.F., Pitfalls in paternity testing. Laboratory Medicine, in “Paternity Testing,” Amer. Soc. Clin. Pathol., p. 28, H.F. Polesky (ed. ), Chicago (1975).
Weiner, A.S., Problems and pitfalls in blood grouping tests for non-parentage. l. Distribution of the blood groups. Amer. J. Clin. Pathol. 41: 9 (1969).
Weiner, A.S., Problems and pitfalls in blood grouping tests for disputed parentage. III. Chances of proving non-paternity by blood grouping tests when the putative father is dead. Acta Genet. Med. Gemmellol 18: 285 (1969).
Boyd, W.C., Compact tubular presentation of mother-child-alleged father combinations which establish non-paternity in the Rh blood group system, Vox. Sang. (OS) 5: 99 (1955).
Allen, F.H., Corcoran, P.A., Kenton, H.B. et al, Mg, a new blood group antigen in the MNS system. Vox. Sang. 3: 81 (1958).
Hopkinson, D.A., Spencer, N. and Harris, H., Red cell acid phosphatase variants: a new human polymorphism, Nature 199: 969 (1963).
Harris, H., Enzyme polymorphisms in man, Proc. Roy. Soc. Lond. 164: 298 (1966).
Fuhrman, W., and Lichte, K.H., Human red cell acid phosphatase polymorphism: a study on gene frequency and forensic use of the system in cases of disputed paternity. Humangenetik 3: 121 (1966).
Giblett, E.R., “Genetic Markers in Human Blood,” F.A. Davis, Philadelphia (1969).
Monn, E., Application of the phosphoglucomutase (PGM) system of human red cells in paternity cases. Vox. Sang. 16: 211 (1969).
Broman, P., Grundin, R. and Lins, P.E., The red cell acid phosphatase polymorphism in Sweden: gene frequencies and application to disputed paternity. Acta Genet. Med. Gemollol. 20: 77 (1971).
Smithies, O., Zone electrophoresis in starch gels; group varia-tions in the serum proteins of normal human adults, Biochem. J. 61: 629 (1955).
Allison, A.C. and Blumberg, B.S., An isoprecipitation reaction distinguishing human serum protein types, Lancet 1: 634 (1961).
Butler, R., Isoantigenicity of human plasma proteins, “Bibliotheca Haematologica” No. 31, S. Karger, Basel (1969).
Prokop, O., Human Blood and Serum Groups, Wiley Interscience, 1969.
Schultz, H.E. and Hermans, J.F.,“Molecular Biology of Human Proteins,” Vol. 1., Elsevier, Amsterdam (1966) p. 173.
Weitkamp, L.R., An electrophoretic comparison of human serum al-bumin variants: Eight distinguishable types. Human Heredity 19: 159, 1969.
Bulletin of the World Health Organization, 35:953 (1966).
Steinberg, A.G., Globulin polymorphisms in man. Ann. Rev. Genet. 3: 25 (1969).
Grubb, R., “The Genetic Markers of Human Immunoglobulins,” Springer-Verla, New York (1970).
Ellis, F.R., Camp, F.R. and Litwin, S.D., “Application of Gm Typing to Paternity Exclusion,” AABB 23rd Ann. Meet., San Francisco (1970).
Allen, F., Corcoran, P.A., Kenton, H.B. Et al, Joint report of Fourth International Histocompatibility Workshop, in “Histocompatibility Testing,” P.I. Terasaki (ed.), Munksgaard, Copenhagen, p. 17 (1970).
Kissmeyer-Nielsen, F., Genetics of the HL-A system in a seminar on histocompatibility testing. Amer. Assoc. Blood Banks, p. 7–20 (1970).
Walford, R.L., A seminar on histocompatibility testing, Amer. Assoc. Blood Banks, p. 37 (1970).
Histocompatibility Testing 1972. Munksgaard.
Lee, C.L., Estimation of the likelihood of paternity, in. “Paternity Testing,” Amer. Soc. Clin. Pathol., p. 28, H.F. Polesky (ed. ), Chicago (1975).
Lombard, J.F., Family law, adoption, paternity and blood tests, Massachusetts Practice, l: part 2, (1967).
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Konugres, A.A. (1976). The Current Status of Paternity Testing. In: Milunsky, A., Annas, G.J. (eds) Genetics and the Law. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-2229-0_19
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DOI: https://doi.org/10.1007/978-1-4684-2229-0_19
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