Familial medullary thyroid carcinoma: Not a distinct entity? Genotype-phenotype correlation in a large family
- 31 December 1996
- journal article
- Published by Elsevier in The American Journal of Medicine
- Vol. 101 (6) , 635-641
- https://doi.org/10.1016/s0002-9343(96)00330-0
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- 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 2AHuman Genetics, 1996
- Activation of RET as a Dominant Transforming Gene by Germline Mutations of MEN2A and MEN2BScience, 1995
- Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor RetNature, 1994
- A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinomaNature, 1994
- Mutations in the RET proto-oncogene are associated with MEN 2A and FMTCHuman Molecular Genetics, 1993
- Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2ANature, 1993
- Familial medullary thyroid carcinoma without associated endocrinopathies: A distinct clinical entityBritish Journal of Surgery, 1986
- STIMULATION OF THYROCALCITONIN SECRETION BY PENTAGASTRIN AND CALCIUM IN TWO PATIENTS WITH MEDULLARY CARCINOMA OF THE THYROID.Journal of Clinical Endocrinology & Metabolism, 1973
- Multiple mucosal neuromas, pheochromocytoma and medullary carcinoma of the thyroid—a syndromeCancer, 1968
- The association of pheochromocytoma with carcinoma of the thyroid glandThe American Journal of Medicine, 1961