Frequent loss of heterozygosity at 6q in pheochromocytoma-Reference-Cited by-同舟云学术

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Frequent loss of heterozygosity at 6q in pheochromocytoma

Published:2006-06 Issue:6 Volume:37 Page:749-754
ISSN:0046-8177
Container-title:Human Pathology
language:en
Short-container-title:Human Pathology

Author:

Lemeta Sebsebe,Salmenkivi Kaisa,Pylkkänen Lea,Sainio Markku,Saarikoski Sirkku T.,Arola Johanna,Heikkilä Päivi,Haglund Caj,Husgafvel-Pursiainen Kirsti,Böhling Tom

Publisher

Elsevier BV

Subject

Pathology and Forensic Medicine

Reference35 articles.

1. How many pathways to pheochromocytoma;Neumann;Semin Nephrol,2002

2. Genetic aspects of pheochromocytoma;Koch;Endocr Regul,2001

3. Inhibin/activin betaB–subunit expression in pheochromocytomas favors benign diagnosis;Salmenkivi;J Clin Endocrinol Metab,2001

4. Benign phaeochromocytoma;McNicol,2004

5. Recent advances in genetics, diagnosis, localization, and treatment of pheochromocytoma;Pacak;Ann Intern Med,2001

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3. Composite tumor with pheochromocytoma and immature neuroblastoma: report of two cases with cytogenetic analysis and discussion of current terminology;Virchows Archiv;2017-09-01

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