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The Application of DNA-Print for the Estimation of Paternity

  • Conference paper
Advances in Forensic Haemogenetics

Part of the book series: Advances in Forensic Haemogenetics ((HAEMOGENETICS,volume 2))

Abstract

We have applied the method of DNA polymorphism analysis to resolve paternity cases. DNA samples were isolated from the blood of mother, child, and alleged father, digested with the restriction endonuclease Pst 1, size separated by agarose gel electrophoresis, and hybridized with four recombinant DNA probes which recognize hypervariable regions in the human genome. Determination of DNA fragment sizes was accomplished with a computer assisted digitizing system. Co-migration of paternally derived DNA fragments in the child and alleged father indicated possible paternity, and a paternity index (PI) was calculated from allele frequency tables accumulated for each polymorphic locus. The cumulative power of exclusion with these four probes, for American Blacks and Caucasians, was on average 99.5% and the mean paternity index more than 3600.

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© 1988 Springer-Verlag Berlin Heidelberg

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Baird, M. et al. (1988). The Application of DNA-Print for the Estimation of Paternity. In: Mayr, W.R. (eds) Advances in Forensic Haemogenetics. Advances in Forensic Haemogenetics, vol 2. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-73330-7_66

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  • DOI: https://doi.org/10.1007/978-3-642-73330-7_66

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-18765-3

  • Online ISBN: 978-3-642-73330-7

  • eBook Packages: Springer Book Archive

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