scholarly article | Q13442814 |
P356 | DOI | 10.1046/J.1365-2265.1999.00648.X |
P698 | PubMed publication ID | 10435055 |
P50 | author | Luis Castaño | Q42278338 |
Guiomar Perez de Nanclares | Q51014984 | ||
P2093 | author name string | E Coto | |
V Alvarez | |||
J Aller | |||
F Díaz-Cadórniga | |||
N Valdés | |||
P2860 | cites work | Clinical studies of multiple endocrine neoplasia type 1 (MEN1) | Q71777163 |
Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states | Q73494435 | ||
Characterization of mutations in patients with multiple endocrine neoplasia type 1. | Q24538768 | ||
Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors | Q24558744 | ||
Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1 | Q28243243 | ||
Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1 | Q28257084 | ||
Positional cloning of the gene for multiple endocrine neoplasia-type 1 | Q28307577 | ||
Definition of the MinimalMEN1Candidate Area Based on a 5-Mb Integrated Map of Proximal 11q13 | Q29303492 | ||
Genetic aspects of adenomatosis of endocrine glands | Q34234754 | ||
Novel germline APC gene mutation in a large familial adenomatous polyposis kindred displaying variable phenotypes | Q34408308 | ||
Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations | Q35611768 | ||
The molecular biology of parathyroid disease | Q36540698 | ||
Pathologic aspects of gastrinomas in patients with Zollinger-Ellison syndrome with and without multiple endocrine neoplasia type I. | Q40712327 | ||
Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11. | Q45094261 | ||
Alleles of the APC gene: an attenuated form of familial polyposis | Q48088124 | ||
Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma | Q48100816 | ||
Somatic mutation of the MEN1 gene in parathyroid tumours. | Q50623754 | ||
Restriction of ocular fundus lesions to a specific subgroup of APC mutations in adenomatous polyposis coli patients. | Q54646990 | ||
P433 | issue | 3 | |
P921 | main subject | multiple endocrine neoplasia | Q1553018 |
multiple endocrine neoplasia type 1 | Q3347154 | ||
P304 | page(s) | 309-313 | |
P577 | publication date | 1999-03-01 | |
P1433 | published in | Clinical Endocrinology | Q15762781 |
P1476 | title | Multiple endocrine neoplasia type 1 (MEN1): clinical heterogeneity in a large family with a nonsense mutation in the MEN1 gene (Trp471Stop) | |
P478 | volume | 50 |
Q37056120 | Causes of death and prognostic factors in multiple endocrine neoplasia type 1: a prospective study: comparison of 106 MEN1/Zollinger-Ellison syndrome patients with 1613 literature MEN1 patients with or without pancreatic endocrine tumors |
Q48935245 | Molecular genetic alterations on chromosomes 11 and 22 in ependymomas |
Q28210134 | The MEN1 gene and associated diseases: an update |
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