Suitability of the YNZ22 (D17S5) VNTR polymorphism for legal medicine investigations in the population of Catalonia (Spain)

Int J Legal Med. 1995;107(4):222-4. doi: 10.1007/BF01428412.

Abstract

Allele and phenotype frequencies for the YNZ22 locus were determined in a population sample from Catalonia (Spain) using the polymerase chain reaction (PCR). In 311 unrelated individuals, 14 alleles and 56 phenotypes were observed. No deviation from Hardy-Weinberg equilibrium was found. The observed heterozygosity was 81.35%. The YNZ22 polymorphism is useful for paternity testing with a CE value of 70% and an Essen-Möller value of 9.35 (log.).

MeSH terms

  • Adult
  • Alleles
  • Child
  • Chromosome Mapping*
  • Chromosomes, Human, Pair 17*
  • DNA Probes*
  • Female
  • Genetic Markers / genetics*
  • Humans
  • Male
  • Minisatellite Repeats / genetics*
  • Paternity*
  • Phenotype
  • Polymerase Chain Reaction / methods
  • Polymorphism, Genetic*
  • Spain

Substances

  • DNA Probes
  • Genetic Markers