Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterised by tumours of the parathyroids, pancreas and anterior pituitary that represents one of the familial cancer syndromes. The MEN1 locus has been previously localised to chromosome 11q13, and a

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Bibliographic Details
Published in:Human molecular genetics 1997-07, Vol.6 (7), p.1177-1183
Main Authors: Lemmens, I, Van de Ven, W J, Kas, K, Zhang, C X, Giraud, S, Wautot, V, Buisson, N, De Witte, K, Salandre, J, Lenoir, G, Pugeat, M, Calender, A, Parente, F, Quincey, D, Gaudray, P, De Wit, M J, Lips, C J, Höppener, J W, Khodaei, S, Grant, A L, Weber, G, Kytölä, S, Teh, B T, Farnebo, F, Thakker, R V
Format: Article
Language:English
Subjects:
Animals
Cattle
Chromosomes, Bacterial
Cloning, Molecular
Cosmids
DNA Mutational Analysis
DNA, Complementary
Female
Gene Library
Humans
Male
Medicin och hälsovetenskap
Multiple Endocrine Neoplasia Type 1 - genetics
Mutation
Neoplasm Proteins - genetics
Proto-Oncogene Proteins
Citations: Items that cite this one
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Description
Summary:Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterised by tumours of the parathyroids, pancreas and anterior pituitary that represents one of the familial cancer syndromes. The MEN1 locus has been previously localised to chromosome 11q13, and a
ISSN:0964-6906
1460-2083
1460-2083
DOI:10.1093/hmg/6.7.1177