Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC
- 1 January 1994
- journal article
- research article
- Published by Springer Science and Business Media LLC in Nature Genetics
- Vol. 6 (1), 70-74
- https://doi.org/10.1038/ng0194-70
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Mutations in the RET proto-oncogene are associated with MEN 2A and FMTCHuman Molecular Genetics, 1993
- Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2Human Molecular Genetics, 1993
- Localisation of the gene for multiple endocrine neoplasia type 2A to a 480 kb region in chromosome band 10q11.2Human Molecular Genetics, 1993
- The spectrum of cystic fibrosis mutationsTrends in Genetics, 1992
- Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2AGenomics, 1991
- Linkage of the multiple endocrine neoplasia type 2B gene (MEN2B) to chromosome 10 markers linked to MEN2AGenomics, 1990
- The Clinical Outcome of Prospective Screening for Multiple Endocrine Neoplasia Type 2AThe New England Journal of Medicine, 1988
- Deletion of genes on chromosome 1 in endocrine neoplasiaNature, 1987
- Familial medullary thyroid carcinoma without associated endocrinopathies: A distinct clinical entityBritish Journal of Surgery, 1986
- Genetic Aspects of Multiple Endocrine NeoplasiaAnnual Review of Medicine, 1984