Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2.

doi:10.1002/gcc.2870060307

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Article

Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2.

Genes, chromosomes & cancer - 1 Mar 1993

Mulligan L M, Gardner E, Smith B A, Mathew C G, Ponder B A

Abstract excerpt

Multiple endocrine neoplasia type 2 (MEN 2) is a familial cancer syndrome arising from mutation at a locus or loci in chromosome region 10p11.2-q11.2. The disease is characterized by medullary thyroid carcinoma (MTC) and pheochromocytoma (Pheo). To assess the genetic events in tumour initiation a...

Topics

Adrenal Gland Neoplasms
Alleles
Carcinoma
Chromosome Mapping
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 10
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 3
DNA Probes
Gene Expression Regulation, Neoplastic
Genes, Tumor Suppressor
Genetic Markers
Genotype
Humans
Multiple Endocrine Neoplasia
Pheochromocytoma
Polymerase Chain Reaction
Thyroid Neoplasms

Source

Open in PubMed

Identifiers

PMID: 7682102
DOI: 10.1002/gcc.2870060307

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-7682102-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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