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Article

Improved carrier testing for multiple endocrine neoplasia, type 1, using new microsatellite-type DNA markers.

Human genetics - 1 Oct 1995

Kytölä S, Leisti J, Winqvist R, Salmela P

Abstract excerpt

Familial multiple endocrine neoplasia, type 1 (FMEN1), is an autosomal dominant trait generated by hyperfunction of various endocrine glands. The gene for MEN1 has been mapped to chromosome 11q13 by genetic linkage and deletion mapping in tumors. Eight Finnish families, including 46 individuals carrying the risk haplotype, have been typed for four polymorphic microsatellite DNA markers spanning the MEN1...

Topics

Alleles
DNA, Satellite
Female
Genetic Markers
Heterozygote
Humans
Male
Multiple Endocrine Neoplasia Type 1
Pedigree

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 7557969
DOI: 10.1007/BF00191805

Genes

MEN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-7557969-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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