Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC-Reference-Cited by-同舟云学术

Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC

Published:1994-01 Issue:1 Volume:6 Page:70-74
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Mulligan Lois M.,Eng Charis,Healey Catherine S.,Clayton David,Kwok John B.J.,Gardner Emily,Ponder Margaret A.,Frilling Andrea,Jackson Charles E.,Lehnert Hendrik,Neumann Hartmut P.H.,Thibodeau Stephen N.,Ponder Bruce A.J.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0194-70.pdf

Reference22 articles.

1. Schimke, R.N. Genetic aspects of multiple endocrine neoplasia. Ann. Rev. Med. 35, 25–31 (1984).

2. Farndon, J.R. et al. Familial medullary thyroid carcinoma without associated endocrinopathies: a distinct clinical entity. Br. J. Surg. 73, 278–281 (1986).

3. Gardner, E. et al. Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2. Hum. molec. Genet. 2, 241–246 (1993).

4. Lairmore, T.C. et al. Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A. Genomics 9, 181–192 (1991).

5. Norum, R.A. et al. Linkage of the multiple endocrine neoplasia type 2B gene (MEN2B) to chromosome 10 markers linked to MEN2A. Genomics 8, 313–317 (1990).

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