Molecular genetics and patient management of multiple endocrine neoplasia type I

Multiple endocrine neoplasia type 1 (MEN-1) is an autosomal dominant disorder characterized by the combined occurrence of tumours of the parathyroids, pancreatic islet cells and anterior pituitary. Other MEN-1-associated tumours include angiofibromas, collagenomas, lipomas, carcinoids and adrenocort...

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Bibliographic Details
Main Author: Thakker, R
Format: Journal article
Language:English
Published: 2001