Multiple endocrine neoplasia type 1 (MEN1), an autosomal dominant disease characterized by neoplasia of the parathyroid glands, anterior pituitary and endocrine pancreas, is rarely reported in Asian populations. The MEN1 gene, mapped to chromosome 11q13 but yet to be cloned, has been found to be hom
Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1)
✍ Scribed by The European Consortium on MEN1; J. H. D. Bassett; A. A. J. Pannett; S. A. Forbes; R. V. Thakker; M. McCarthy; A. P. Read; B. T. Teh; C. Larsson; S. Kytölä; J. Leisti; P. Salmela; G. Weber; S. Giraud; C. X. Zhang; A. Calender; J. W. M. Höppener; H. K. Ploos van Amstel; C. J. M. Lips; K. Kas; W. J. M. Van de Ven; P. Gaudray
- Publisher
- Springer
- Year
- 1997
- Tongue
- English
- Weight
- 65 KB
- Volume
- 100
- Category
- Article
- ISSN
- 0340-6717
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## Abstract ## BACKGROUND Multiple endocrine neoplasia type 1 (MEN 1) is an autosomal‐dominant syndrome associated with neoplasia of pituitary, pancreas, parathyroid, and foregut lineage neuroendocrine tissue. Although enteropancreatic carcinoid has been well described in patients with MEN 1, it w