Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

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...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alleles
Share to Child
Share to Chromosome Mapping

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to DNA Probes

Share to Genetic Markers

Share to Phenotype

Share to Polymerase Chain Reaction

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 7599103
DOI: 10.1007/BF01428412

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

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

The allele frequency distribution at VNTR locus D17S5 (YNZ22) in a Japanese population sample.Semantic proximity Read ↗

Allele frequencies for the VNTR locus D17S5 (YNZ22) in Hungary.Semantic proximity Read ↗

PCR typing of the locus D17S30 (YNZ22 VNTR) in an Italian population sample.Semantic proximity Read ↗

PCR amplification of large VNTR alleles of D17S5 (YNZ22) locus.Semantic proximity Read ↗

Polymorphism analysis of the VNTR locus D17S5 in central Spain.Semantic proximity Read ↗

Rapid typing of 4 VNTR loci, 3'ApoB, MCT118,St14 and YNZ22 by the polymerase chain reaction of a Greek sample.Semantic proximity Read ↗

Catalonian population study of the tetranucleotide repeat loci D3S1358, D8S1179, D18S51 and D19S253.Semantic proximity Read ↗

Population study of the STRs HUMCD4 and HUMF13A1 in Catalonia (Northeast Spain).Semantic proximity Read ↗

Population study of the STRs HUMTH01 (including a new variant) and HUMVWA31A in Catalonia (northeast Spain).Semantic proximity Read ↗

Y-chromosome variation in a Norwegian population sample.Semantic proximity Read ↗

Polymerase chain reaction (PCR) amplification of hypervariable genomic sequences.Semantic proximity Read ↗

[Use of DNA amplification by PCR in the study of the hypervariable region (VNTR) in a forensic medicine setting. Experience with 2 systems: Apo B and YNZ 22].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.