The RET protooncogene in sporadic pheochromocytomas: frequent MEN 2-like mutations and new molecular defects.-Reference-Cited by-同舟云学术

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The RET protooncogene in sporadic pheochromocytomas: frequent MEN 2-like mutations and new molecular defects.

Published:1995-07 Issue:7 Volume:80 Page:2063-2068
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

Beldjord C,Desclaux-Arramond F,Raffin-Sanson M,Corvol J C,De Keyzer Y,Luton J P,Plouin P F,Bertagna X

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/80/7/2063/10505378/jcem2063.pdf

Cited by 3 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. New Insights into the Genetics of Familial Chromaffin Cell Tumors;Annals of the New York Academy of Sciences;2002-09

2. Somatic VHL gene deletion and point mutation in MEN 2A-associated pheochromocytoma;Oncogene;2002-01

3. RET Proto-Oncogene in the Development of Human Cancer;Journal of Clinical Oncology;1999-01

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