A <I>RET </I>Mutation with Decreased Penetrance in the Family of a Patient with a-Reference-Cited by-同舟云学术

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A RET Mutation with Decreased Penetrance in the Family of a Patient with a

Published:2005 Issue:2 Volume:28 Page:193-198
ISSN:0969-711X
Container-title:Endocrine
language:en
Short-container-title:ENDO

Author:

Arum Seth M.,Dahia Patricia L. M.,Schneider Katherine,Braverman Lewis E.

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://www.springerlink.com/index/pdf/10.1385/ENDO:28:2:193

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Long‐term follow‐up of RET Y791F carriers in Denmark 1994‐2017: A National Cohort Study;Journal of Surgical Oncology;2019-01-15

2. Questioning the pathogenic role of the pTyr791Phe mutation of the RET proto-oncogene: Insight from a case report;Annales d'Endocrinologie;2015-12

3. Prevalence by Age and Predictors of Medullary Thyroid Cancer in Patients with Lower Risk Germline RET Proto-Oncogene Mutations;Thyroid;2014-07

4. Comprehensive analysis of RET gene should be performed in patients with multiple endocrine neoplasia type 2 (MEN 2) syndrome and no apparent genotype- phenotype correlation: An appraisal of p.Y791F and p.C634Y RET mutations in five unrelated Brazilian families;J ENDOCRINOL INVEST;2013

5. High Penetrance of Pheochromocytoma Associated with the Novel C634Y/Y791F Double Germline Mutation in theRETProtooncogene;The Journal of Clinical Endocrinology & Metabolism;2010-03-01

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