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

Spectrum of genetic alterations in Muir‐Torre syndrome is the same as in HNPCC

29 Sept 2003

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Cancer Genomics and Diagnostics
Share to Colorectal and Anal Carcinomas
Share to Genetic factors in colorectal cancer

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 14994245
DOI: 10.1002/ajmg.a.20523

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Spectrum of genetic alterations in Muir‐Torre syndrome is the same as in HNPCCPMID 14994245Read ↗

HNPCC (Lynch Syndrome): Differential Diagnosis, Molecular Genetics and Management - a ReviewSemantic proximity Read ↗

Peutz-Jeghers syndrome: clinicopathology and molecular alterationsSemantic proximity Read ↗

Acute myeloid leukaemia associated with Muir-Torre variant of hereditary non-polyposis colon cancer (HNPCC): implications for inherited and acquired mutations in DNA mismatch repair genes.Semantic proximity Read ↗

MSH6 mutation in Muir-Torre syndrome: could this be a rare finding?Semantic proximity Read ↗

An update of HNPCC (Lynch syndrome)Semantic proximity Read ↗

Human nucleotide excision repair syndromes: molecular clues to unexpected intricacies.Semantic proximity Read ↗

Comprehensive characterization of HNPCC-related colorectal cancers reveals striking molecular features in families with no germline mismatch repair gene mutationsSemantic proximity Read ↗

Clinical and Molecular Features of Skin Malignancies in Muir-Torre Syndrome.Semantic proximity Read ↗

MSI test to distinguish between HNPCC and other predisposing syndromes -- of value in tailored surveillance.Semantic proximity Read ↗

Lynch syndrome - Muir-Torre variant: implication in gynecologic oncology.Semantic proximity Read ↗

Skin lesions with Lynch syndrome could represent Muir-Torre syndrome.Semantic proximity Read ↗

Muir-Torre syndrome: case report and molecular characterization.Semantic proximity Read ↗

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