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

[Clinical significance and strategies to analyze genetic polymorphisms].

Rinsho byori. The Japanese journal of clinical pathology - 1 Feb 2001

Murata M

Abstract excerpt

A DNA polymorphism can be defined as a difference in the primary sequence of DNA, and the frequency of the rarer allele among the general population exceeds 1%. Several types of polymorphisms, including minisatellite and microsatellite markers, deletion or insertion of short nucleotide sequences, and single nucleotide polymorphisms(SNPs), are present in human genome, with different frequencies and different...

Read the complete abstract on PubMed

Topics

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

Share to Genetic Predisposition to Disease
Share to Polymorphism, Genetic
Share to Polymorphism, Single Nucleotide

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

Source

Identifiers

PMID: 11307307

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

[Clinical significance and strategies to analyze genetic polymorphisms].PMID 11307307Read ↗

[DNA polymorphisms].Semantic proximity Read ↗

[Important role of single nucleotide polymorphisms in the study of complex diseases].Semantic proximity Read ↗

[Genetic variation studies a breakthrough in the understanding of many common diseases].Semantic proximity Read ↗

[The development and clinical implication of genetic tests].Semantic proximity Read ↗

[Genetic polymorphisms: how to interpret studies?].Semantic proximity Read ↗

Role of genetic variability in Mendelian and multifactorial diseases.Semantic proximity Read ↗

Genetic polymorphisms and implications for human diseases.Semantic proximity Read ↗

[Structural variation in the human genome].Semantic proximity Read ↗

[Genome-wide analysis of single nucleotide polymorphisms].Semantic proximity Read ↗

[Statistical analysis of genetic polymorphisms in epidemiological studies].Semantic proximity Read ↗

Genetic variation analysis for biomedical researchers: a primer.Semantic proximity Read ↗

[Analysis of single nucleotide polymorphisms (SNPs)].Semantic proximity Read ↗

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