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Article

Genotype-phenotype analysis in multiple endocrine neoplasia type 1.

Archives of surgery (Chicago, Ill. : 1960) - 1 Jun 2002

Kouvaraki Maria A, Lee Jeffrey E, Shapiro Suzanne E, Gagel Robert F, Sherman Steven I, Sellin Rena V, Cote Gilbert J, Evans Douglas B

Abstract excerpt

HYPOTHESIS: Multiple endocrine neoplasia type 1 (MEN 1) syndrome is an autosomal dominant disorder caused by germline mutations in the MEN1 gene and characterized by multiple endocrine tumors, most notably in the parathyroid glands, pituitary, and pancreas. The syndrome demonstrates variable expressivity and considerable genetic heterogeneity. Patient data were examined for possible associations between genotype...

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Source

Identifiers

PMID: 12049533
DOI: 10.1001/archsurg.137.6.641

Genes

MEN1

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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.

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