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

Familial adenomatous polyposis associated craniopharyngioma secondary to both germline and somatic mutations in the APC gene.

Acta neuropathologica - 1 Dec 2020

Passos Jeremy, Quidet Mathilde, Brahimi Afane, Flament Cathy, Gibier Jean-Baptiste, Caron Sabine, Maurage Claude-Alain, Buisine Marie-Pierre, Perbet Romain

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 Adenomatous Polyposis Coli
Share to Craniopharyngioma
Share to Genes, APC

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Germ-Line Mutation

Share to Mutation

Share to Pituitary Neoplasms

Source

Identifiers

PMID: 33025138
DOI: 10.1007/s00401-020-02232-9

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

Familial adenomatous polyposis associated craniopharyngioma secondary to both germline and somatic mutations in the APC gene.PMID 33025138Read ↗

Second-hit APC mutation in a familial adamantinomatous craniopharyngioma.Semantic proximity Read ↗

Medulloblastomas associated with an APC germline pathogenic variant share the good prognosis of CTNNB1-mutated medulloblastomasSemantic proximity Read ↗

Brain tumors in individuals with familial adenomatous polyposis: a cancer registry experience and pooled case report analysis.Semantic proximity Read ↗

APC and CTNNB1 mutations are rare in sporadic ependymomas.Semantic proximity Read ↗

Common mutations of beta-catenin in adamantinomatous craniopharyngiomas but not in other tumours originating from the sellar region.Semantic proximity Read ↗

Somatic mutations of WNT/wingless signaling pathway components in primitive neuroectodermal tumors.Semantic proximity Read ↗

Multiple gynecologic tumors as rare associated phenotypes of FAP/Gardner syndrome in a family with the novel germline mutation in the APC gene.Semantic proximity Read ↗

Beta-catenin mutations in craniopharyngiomas and pituitary adenomas.Semantic proximity Read ↗

APC mutations in sporadic medulloblastomas.Semantic proximity Read ↗

Germline Mutations of the APC Gene in Patients with Familial Adenomatous Polyposis-Associated Thyroid Carcinoma: Results from a European Cooperative StudySemantic proximity Read ↗

Prolactinoma as the first manifestation of Gardner's syndrome.Semantic proximity Read ↗

Mutations of the adenomatous polyposis coli and p53 genes in a child with Turcot's syndrome.Semantic proximity Read ↗

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