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

Analysis of eight polymorphic human genetic markers in a well-defined Greek population.

The American journal of forensic medicine and pathology - 1 Jun 2000

Tsopanomichalou M, Sourvinos G, Arvanitis D, Michalodimitrakis M

Abstract excerpt

The use of DNA in forensic science has become a basic tool for person identification or parentage testing. The use of polymorphic markers permits the formation of a unique profile for each individual. The knowledge of allele frequencies in a given population allows the scientist to estimate the probability of a particular allele combination. For this task, allele databanks are essential. In this report, the...

Read the complete abstract on PubMed

Topics

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

Share to Forensic Medicine
Share to Gene Frequency
Share to Genetic Markers

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

Share to Genetics, Population

Share to Greece

Share to Minisatellite Repeats

Share to Polymorphism, Genetic

Share to White People

Source

Identifiers

PMID: 10871135
DOI: 10.1097/00000433-200006000-00016

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

Analysis of eight polymorphic human genetic markers in a well-defined Greek population.PMID 10871135Read ↗

Genetic variation at six STR loci (HUMTH01, HUMTPOX, HUMCSF1PO, HUMF13A01, HUMFES/FPS, HUMVWFA31) in Aragon (north Spain).Semantic proximity Read ↗

Genetic variation of 15 autosomal STR loci in Upper (Southern) Egyptians.Semantic proximity Read ↗

Hungarian population data on six STR loci--HUMVWFA31, HUMTH01, HUMCSF1PO, HUMFES/FPS, HUMTPOX, and HUMHPRTB--derived using multiplex PCR amplification and manual typing.Semantic proximity Read ↗

Allele frequencies for 13 STRs loci in a Western Anatolia population and their forensic evaluation.Semantic proximity Read ↗

Genetic variation for 15 autosomal STR loci (PowerPlex 16) in a population sample from northern Greece.Semantic proximity Read ↗

Analysis of the HUMTH01 allele frequencies in the Spanish population.Semantic proximity Read ↗

Allele frequency distribution of four PCR-amplified loci in the Spanish population.Semantic proximity Read ↗

Turkish population data on nine short tandem repeat loci: HumCSF1PO, HumTHO1, HumTPOX, HumFES/FPS, HumF13B, HumVWA, D3S1358, D7S820, D16S539.Semantic proximity Read ↗

Semi-automatic DNA profiling in a Hungarian Romany population using the STR loci HumVWFA31, HumTH01, HumTPOX, and HumCSF1PO.Semantic proximity Read ↗

Allele frequency distributions of 13 PCR-based systems in a population from North-East Spain.Semantic proximity Read ↗

Population genetics of the STR loci HUMCSF1PO, HUMF13A01, HUMFES/FPS and D12S391 in Asturias (northern Spain).Semantic proximity Read ↗

Distribution of HumvWA31, HumFESFPS, HumTH01, HumTPOX, HumCD4, HumCSF1PO alleles in a Southern Italian population sample.Semantic proximity Read ↗

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