| P50 | author | Bin Tean Teh | Q47451223 |
| P2093 | author name string | Shepherd J | |
| | Walters M | |
| | Cameron D | |
| | Palmer J | |
| | Hayward N | |
| | Bergman L | |
| | Cardinal J | |
| P2860 | cites work | Multiple facial angiofibromas and collagenomas in patients with multiple endocrine neoplasia type 1 | Q73543135 |
| | Pathology of MEN-1: morphology, clinicopathologic correlations and tumour development | Q74817182 |
| | Novel V184E MEN1 germline mutation in a Japanese kindred with familial hyperparathyroidism | Q77647381 |
| | Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases | Q77794377 |
| | Germline mutation of the multiple endocrine neoplasia type 1 (MEN1) gene in a family with primary hyperparathyroidism | Q77965881 |
| | Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription | Q22001458 |
| | Characterization of mutations in patients with multiple endocrine neoplasia type 1. | Q24538768 |
| | A simple salting out procedure for extracting DNA from human nucleated cells | Q27861086 |
| | Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1 | Q28243243 |
| | Positional cloning of the gene for multiple endocrine neoplasia-type 1 | Q28307577 |
| | Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders | Q34386474 |
| | Multiple endocrine neoplasia type I: clinical syndrome to molecular genetics | Q40375094 |
| | A family with isolated hyperparathyroidism segregating a missense MEN1 mutation and showing loss of the wild-type alleles in the parathyroid tumors | Q43217979 |
| | Germline mutations in the MEN1 gene: creation of a new splice acceptor site and insertion of 7 intron nucleotides into the mRNA. | Q47917547 |
| | Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma | Q48100816 |
| | A large germline deletion of the MEN1 gene in a family with multiple endocrine neoplasia type 1. | Q54960820 |
| | Germline mutations of the MEN1 gene in Japanese kindred with multiple endocrine neoplasia type 1. | Q55099861 |
| | Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism | Q58862086 |
| | Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states | Q73494435 |
| P433 | issue | 8 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1009-1014 | |
| P577 | publication date | 2000-10-01 | |
| P1433 | published in | British Journal of Cancer | Q326309 |
| P1476 | title | Identification of MEN1 gene mutations in families with MEN 1 and related disorders | |
| P478 | volume | 83 | |