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Mutation analysis of the RET proto-oncogene in Dutch families with MEN 2A, MEN 2B and FMTC: two novel mutations and one de novo mutation for MEN 2A

✍ Scribed by Landsvater, RudyM.; Jansen, RumoP.M.; Hofstra, RobertM.W.; Buys, CharlesH.C.M.; Lips, CornelisJ.M.; Amstel, HansKristianPloos

Book ID
118771704
Publisher
Springer
Year
1996
Tongue
English
Weight
532 KB
Volume
97
Category
Article
ISSN
0340-6717

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πŸ“œ SIMILAR VOLUMES

Diagnosis of multiple endocrine neoplasi
Diagnosis of multiple endocrine neoplasia [MEN] 2A, 2B and familial medullary thyroid cancer [FMTC] by multiplex PCR and heteroduplex analyses of RET proto-oncogene mutations
✍ Marios Kambouris; Charles E. Jackson; Gerald L. Feldman πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 1006 KB

Communicated by B w e A.J. Pondei Multiple endocrine neoplasia type 2 [MEN 21 is an autosomal dominant cancer syndrome with two subtypes, 2A and 2B. MEN 2A and medullary thyroid cancer [MTC] are caused by >25 different point mutations in exons 10, 11, and 13 of the RET proto-oncogene, whereas MEN 2B