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

Multiple basal cell carcinomas revealing a biallelic MUTYH gene mutation in a 39-year-old male patient.

Journal of the European Academy of Dermatology and Venereology : JEADV - 1 Mar 2023

Tzoumpa Sofia, Sevenet Nicolas, Bejar-Ardiles Claudia-Luisa, Villette Béatrice, Zumelzu Coralie, Benamouzig Robert, Caux Frédéric, Maubec Eve

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 Colorectal Neoplasms
Share to Genetic Predisposition to Disease
Share to Germ-Line Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Source

Identifiers

PMID: 36151995
DOI: 10.1111/jdv.18592

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Multiple basal cell carcinomas revealing a biallelic MUTYH gene mutation in a 39-year-old male patient.PMID 36151995Read ↗

A second case report of medulloblastoma in a patient carrying biallelic pathogenic MUTYH germline variants.Semantic proximity Read ↗

Non-syndromic hereditary basal cell carcinomas: a reduplicated discovery.Semantic proximity Read ↗

Novel BRCA2 mutation in a Polish family with hamartoma and two male breast cancers.Semantic proximity Read ↗

Multiple squamous cell carcinomas arising on an epidermal nevus harboring HRAS p.G13R mutation.Semantic proximity Read ↗

[Basal cell carcinoma. Molecular genetics and unusual clinical features].Semantic proximity Read ↗

Breast cancers in monoallelic MUTYH germline mutation carriers have clinicopathological features overlapping with those in BRCA1 germline mutation carriers.Semantic proximity Read ↗

Hereditary Cancer Syndrome in a Family with Double Mutation in BRIP1 and MUTYH Genes.Semantic proximity Read ↗

Clinicopathological and molecular spectrum of patients with germline SUFU mutations: A case series.Semantic proximity Read ↗

Common genetic variants of MUTYH are not associated with cutaneous malignant melanoma: application of molecular screening by means of high-resolution melting technique in a pilot case-control study.Semantic proximity Read ↗

Letter to the editor: rectal cancer in a 15-year-old female with a novel MLH1 and MSH6 biallelic inheritance.Semantic proximity Read ↗

Coincident two mutations and one single nucleotide polymorphism of the PTCH1 gene in a family with naevoid basal cell carcinoma syndrome.Semantic proximity Read ↗

Multiple basal cell carcinomas in a 38-year-old woman with Goltz syndrome.Semantic proximity Read ↗

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