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The variable penetrance and spectrum of manifestations of multiple endocrine neoplasia type 1

✍ Scribed by Sally E. Carty; Audrey K. Helm; Janet A. Amico; Martha R. Clarke; Thomas P. Foley; Charles G. Watson; John J. Mulvihill


Book ID
117849052
Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
55 KB
Volume
124
Category
Article
ISSN
0039-6060

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## Abstract Multiple endocrine neoplasia type 1 (MEN1) is an inherited cancer predisposition syndrome typified by development of tumors in parathyroid, pituitary and endocrine pancreas, as well as less common sites including both endocrine and nonendocrine organs. Deletion or mutation of the tumor