Related Articles
Genetic analysis and clinical investigation of a pedigree with multiple endocrine neoplasia type 2A: A case report
Clinical significance of RET mutation screening in a pedigree of multiple endocrine neoplasia type 2A
Evaluation of the role of RET polymorphisms/haplotypes as modifier loci for MEN 2, and analysis of the correlation with the type of RET mutation in a series of Spanish patients
CGH alterations in medullary thyroid carcinomas in relation to the RET M918T mutation and clinical outcome
Analysis of somatic mutations in braf, CDKN2A/p16 and PI3KCA in patients with medullary thyroid carcinoma