RET gene mutations (genotype and phenotype) of multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma
Author:
Affiliation:
1. Stanford University School of Medicine; Stanford California
Publisher
Wiley
Subject
Cancer Research,Oncology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/cncr.28661/fullpdf
Reference136 articles.
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3. Evidence of MEN-2 in the original description of classic pheochromocytoma;Neumann;N Engl J Med.,2007
4. Study of a kindred with pheochromocytoma, medullary thyroid carcinoma, hyperparathyroidism and Cushing's disease: multiple endocrine neoplasia, type 2;Steiner;Medicine (Baltimore).,1968
5. Multiple endocrine neoplasia type 2;Sizemore;Clin Endocrinol Metab.,1980
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