Germline sequence variant S836S in the RET proto-oncogene is associated with low level predisposition to sporadic medullary thyroid carcinoma in the Spanish population-Reference-Cited by-同舟云学术

Germline sequence variant S836S in the RET proto-oncogene is associated with low level predisposition to sporadic medullary thyroid carcinoma in the Spanish population

Published:2001-09 Issue:3 Volume:55 Page:399-402
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:

Author:

Ruiz Agustín,Antiñolo Guillermo,Fernández Raquel M.,Eng Charis,Marcos Irene,Borrego Salud

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2265.2001.01328.x/fullpdf

Reference13 articles.

1. Molecular analysis of the RET and GDNF genes in a family with multiple endocrine neoplasia type 2A and Hirschsprung disease;Borrego;Journal of Clinical Endocrinology and Metabolism,1998

2. Specific polymorphisms in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expression;Borrego;Journal of Medical Genetics,1999

3. RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease;Borrego;Journal of Medical Genetics,2000

4. Mutation of the RET protooncogene in sporadic medullary thyroid carcinoma;Eng;Genes, Chromosomes and Cancer,1995

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