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

Clinical testing for mutations in the MEN1 gene in Sweden: a report on 200 unrelated cases.

The Journal of clinical endocrinology and metabolism - 1 Sept 2007

Tham Emma, Grandell Ulla, Lindgren Eva, Toss Göran, Skogseid Britt, Nordenskjöld Magnus

Abstract excerpt

CONTEXT: Multiple endocrine neoplasia type 1 (MEN1) is a tumor syndrome of the parathyroid, endocrine pancreas, and anterior pituitary caused by mutations in the MEN1 gene on 11q13. OBJECTIVE: The goal of this study was to determine the MEN1 mutation spectrum and detection rate among Swedish patients and identify which patient categories should be tested for MEN1 mutations. DESIGN/SETTING/PATIENTS: DNA sequences...

Read the complete abstract on PubMed

Topics

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

Share to Aged, 80 and over
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Multiple Endocrine Neoplasia Type 1

Share to Pancreatic Neoplasms

Share to Parathyroid Neoplasms

Share to Proto-Oncogene Proteins

Share to Sweden

Source

Identifiers

PMID: 17623761
DOI: 10.1210/jc.2007-0476

Genes

MEN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical testing for mutations in the MEN1 gene in Sweden: a report on 200 unrelated cases.PMID 17623761Read ↗

Clinical testing for multiple endocrine neoplasia type 1 in a DNA diagnostic laboratory.Semantic proximity Read ↗

Detection of an MEN1 gene mutation depends on clinical features and supports current referral criteria for diagnostic molecular genetic testing.Semantic proximity Read ↗

Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the geneSemantic proximity Read ↗

Analysis of gross deletions in the <i>MEN1</i> gene in patients with multiple endocrine neoplasia type 1Semantic proximity Read ↗

The MEN1 gene and associated diseases: an update.Semantic proximity Read ↗

UMD-MEN1 Database: An Overview of the 370 MEN1 Variants Present in 1676 Patients From the French PopulationSemantic proximity Read ↗

Menin mutations in the diagnosis and prediction of multiple endocrine neoplasia type 1.Semantic proximity Read ↗

A novel deletion of the MEN1 gene in a large family of multiple endocrine neoplasia type 1 (MEN1) with aggressive phenotype.Semantic proximity Read ↗

Genotype-phenotype analysis in multiple endocrine neoplasia type 1.Semantic proximity Read ↗

One genotype with a myriad of phenotypes: A family with multiple endocrine neoplasia.Semantic proximity Read ↗

A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testing.Semantic proximity Read ↗

Analysis of genotype-phenotype correlations and survival outcomes in patients with primary hyperparathyroidism caused by multiple endocrine neoplasia type 1: the experience at a single institution.Semantic proximity Read ↗

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