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Article

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

International journal of legal medicine - 1 Jan 1995

Gené M, Huguet E, Sánchez-García C, Moreno P, Corbella J, Mezquita J

Abstract excerpt

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...

Topics

Adult
Alleles
Child
Chromosome Mapping
Chromosomes, Human, Pair 17
DNA Probes
Female
Genetic Markers
Humans
Male
Minisatellite Repeats

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Paternity

Phenotype

Polymerase Chain Reaction

Polymorphism, Genetic

Spain

Source

Identifiers

PMID: 7599103
DOI: 10.1007/BF01428412

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-7599103-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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Suitability of the YNZ22 (D17S5) VNTR polymorphism for legal medicine investigations in the population of Catalonia (Spain).PMID 7599103Read ↗

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