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RET gene mutations (genotype and phenotype) of multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma

โœ Scribed by Krampitz, Geoffrey W.; Norton, Jeffrey A.


Book ID
121729218
Publisher
John Wiley and Sons
Year
2014
Tongue
English
Weight
277 KB
Volume
120
Category
Article
ISSN
0008-543X

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Detection of RET mutations in multiple e
โœ Michael L. Peacock; Marilyn J. Borst; Jason D. Sweet; Ruth A. Decker ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 465 KB ๐Ÿ‘ 1 views

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