Abstract
Before the developement of DNA polymorphism the most cases of disputed paternity were solved by testing blood groups, serum proteins, erythrocyte enzymes and additionally HLA. Nevertheless in cases of only one system exclusion, especially homozygotic ones, or silent genes the further extension of surveys, family investigations or finally investigation of the enzyme activity has been required. Those cases have been suggested by some authors to be resolved using the DNA technique [4,7,8,10]. Since Nakamura et al. [9] had reported the polymorphic region — VNTR locus D1S80 and Kasai et al. [3] had sequenced it the new approach caused by the introduction of D1S80 into disputed paternity investigation has been used.
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© 1995 Springer-Verlag Berlin Heidelberg
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Miścicka-Śliwka, D., Śliwka, K., Syroczyńska, A., Berent, J.A. (1995). Usefulness of D1S80 System in Paternity Investigation. In: Mangin, P., Ludes, B. (eds) Acta Medicinæ Legalis Vol. XLIV 1994. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-79523-7_23
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DOI: https://doi.org/10.1007/978-3-642-79523-7_23
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