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Polyclonal origin of medullary carcinoma of the thyroid in multiple endocrine neoplasia type 2

✍ Scribed by A. M. Ferraris; Rosa Mangerini; Gian Franco Gaetani; Cristina Romei; Aldo Pinchera; Furio Pacini

Publisher
Springer
Year
1997
Tongue
English
Weight
50 KB
Volume
99
Category
Article
ISSN
0340-6717

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Communicated by Kenneth K. Kidd Gennline missense mutations within the coding region of the RET proto-oncogene have recently been described in patients with the dominantly inherited cancer syndromes, multiple endocrine neoplasia type 2a (MEN 2a) and familial medullary thyroid carcinoma (FMTC). To da