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Article

Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2).

European journal of human genetics : EJHG - 1 Sept 2010

Rahner Nils, Steinke Verena, Schlegelberger Brigitte, Olschwang Sylviane, Eisinger François, Hutter Pierre

Abstract excerpt

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Read the complete abstract on PubMed

Topics

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Share to Adaptor Proteins, Signal Transducing
Share to Adenosine Triphosphatases
Share to Colorectal Neoplasms, Hereditary Nonpolyposis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Repair Enzymes

Share to Germany

Share to Mismatch Repair Endonuclease PMS2

Share to MutL Protein Homolog 1

Share to MutS Homolog 2 Protein

Source

Open in PubMed Open full text

Identifiers

PMID: 20104243
DOI: 10.1038/ejhg.2009.232
PMCID: PMC2987434

Genes

MLH1
MSH2
MSH6
PMS2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

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Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2).PMID 20104243Read ↗

Clinical utility gene card for: Lynch syndrome (MLH1, MSH2, MSH6, PMS2, EPCAM) - update 2012.Semantic proximity Read ↗

Identification of Lynch Syndrome.Semantic proximity Read ↗

Identification of new genetic alterations in MLH1, MSH2 and MSH6 using IHC and HRM analysis in Lynch syndrome-suspected patientsSemantic proximity Read ↗

Update on Lynch syndrome genomics.Semantic proximity Read ↗

The changing landscape of Lynch syndrome due to PMS2 mutations.Semantic proximity Read ↗

Clinical utility gene card for: Meckel syndrome - update 2016.Semantic proximity Read ↗

Lynch syndrome, molecular mechanisms and variant classification.Semantic proximity Read ↗

Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch SyndromeSemantic proximity Read ↗

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome DatabaseSemantic proximity Read ↗

The guidelines for clinical practice for carriers of germline mutations in the Lynch syndrome predisposition genes MLH1, MSH2, MSH6, PMS2 and large deletions of EPCAM (4.2024).Semantic proximity Read ↗

Clinical utility gene card for: MUTYH-associated polyposis (MAP), autosomal recessive colorectal adenomatous polyposis.Semantic proximity Read ↗

Integrated analysis of unclassified variants in mismatch repair genes.Semantic proximity Read ↗

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