Characteristic genomic imbalances in pediatric pheochromocytoma-Reference-Cited by-同舟云学术

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Characteristic genomic imbalances in pediatric pheochromocytoma

Published:2006 Issue:6 Volume:45 Page:602-607
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosom. Cancer

Author:

Hering Antje,Guratowska Monika,Bucsky Peter,Claussen Uwe,Decker Jochen,Ernst Guenther,Hoeppner Wolfgang,Michel Susanne,Neumann Hartmut,Parlowsky Thomas,Loncarevic Ivan

Publisher

Wiley

Subject

Cancer Research,Genetics

Reference36 articles.

1. Microarray-based CGH of sporadic and syndrome-related pheochromocytomas using a 0.1-0.2 Mb bacterial artificial chromosome array spanning chromosome arm 1p

2. VHL c.505 T>C mutation confers a high age related penetrance but no increased overall mortality

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4. Profiling of Somatic Mutations in Phaeochromocytoma and Paraganglioma by Targeted Next Generation Sequencing Analysis;International Journal of Endocrinology;2015

5. Bilateral Pheochromocytomas, Hemihyperplasia, and Subtle Somatic Mosaicism: The Importance of Detecting Low-Level Uniparental Disomy;American Journal of Medical Genetics Part A;2013-03-26

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