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 multiple endocrine neoplasia type 1 in a DNA diagnostic laboratory.

Genetics in medicine : official journal of the American College of Medical Genetics - 1 Feb 2005

Klein Roger D, Salih Sana, Bessoni Jesse, Bale Allen E

Abstract excerpt

PURPOSE: Based on results of diagnostic MEN1 testing, we have attempted to further define the mutational spectrum of the MEN1 gene and the clinical features most frequently associated with MEN1 mutations. METHODS: Mutation testing was performed on blood samples by PCR amplification and sequencing of exons 2 to 10 of the MEN1 gene and the corresponding intron-exon junctions. Pedigree phenotypic information was...

Read the complete abstract on PubMed

Topics

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

Share to DNA Mutational Analysis
Share to Genes, Tumor Suppressor

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hyperparathyroidism

Share to Multiple Endocrine Neoplasia Type 1

Share to Pancreatic Neoplasms

Share to Pedigree

Share to Polymerase Chain Reaction

Share to Proto-Oncogene Proteins

Source

Identifiers

PMID: 15714081
DOI: 10.1097/01.gim.0000153663.62300.f8

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 multiple endocrine neoplasia type 1 in a DNA diagnostic laboratory.PMID 15714081Read ↗

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

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

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

Screening of the Men1 gene and discovery of germ-line and somatic mutations in apparently sporadic parathyroid tumors.Semantic proximity Read ↗

Multiple endocrine neoplasia type 1 (MEN1): not only inherited endocrine tumors.Semantic proximity Read ↗

Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related statesSemantic proximity Read ↗

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

Clinical Practice Guidelines for Multiple Endocrine Neoplasia Type 1 (MEN1)Semantic proximity Read ↗

Screening for MEN1 mutations in patients with atypical endocrine neoplasia.Semantic proximity Read ↗

MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1.Semantic proximity Read ↗

Multiple Endocrine Neoplasia: Genetics and Clinical Management.Semantic proximity Read ↗

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