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

Phenotypic Variability of MUTYH-Associated Polyposis in Monozygotic Twins and Endoscopic Resection of A Giant Polyp in Pregnancy.

The American journal of gastroenterology - 1 Apr 2018

Casper Markus, Spier Isabel, Holz Robert, Aretz Stefan, Lammert Frank

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 Polyps
Share to Colorectal Neoplasms
Share to DNA Glycosylases
Share to Germ-Line Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pregnancy

Share to Pregnancy Complications, Neoplastic

Share to Tumor Burden

Share to Twins, Monozygotic

Source

Identifiers

PMID: 29610499
DOI: 10.1038/ajg.2018.19

Genes

MUTYH

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Phenotypic Variability of MUTYH-Associated Polyposis in Monozygotic Twins and Endoscopic Resection of A Giant Polyp in Pregnancy.PMID 29610499Read ↗

MUTYH associated polyposis coli: one common and one rare mutation.Semantic proximity Read ↗

Multi-gene panel testing confirms phenotypic variability in MUTYH-Associated PolyposisSemantic proximity Read ↗

The mysteries of mosaicism: phenotypic variability in a family with incontinentia pigmenti.Semantic proximity Read ↗

Clinical Spectrum and Science Behind the Hamartomatous Polyposis SyndromesSemantic proximity Read ↗

Type and frequency of MUTYH variants in Italian patients with suspected MAP: a retrospective multicenter study.Semantic proximity Read ↗

Somatic mutation, a cause of biliary atresia: A hypothesis.Semantic proximity Read ↗

Isolated fetal macrodactyly: phenotypic and genetic disparities in mosaic overgrowth syndrome.Semantic proximity Read ↗

Kindler syndrome with a novel mutation and gynaecological complication.Semantic proximity Read ↗

Waardenburg syndrome: variable phenotypic expression in monozygotic twins.Semantic proximity Read ↗

Excessive Weight Loss in a Neonate - Novel Mutation Causing Primary Hypoaldosteronism.Semantic proximity Read ↗

Phenotypic heterogeneity associated with a novel MECOM variant: Mild thrombocytopenia to hydrops fetalis.Semantic proximity Read ↗

Prenatal phenotypic discordance in monozygotic twins due to a postzygotic TSC2 variant.Semantic proximity Read ↗

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