Using GeneReader NGS system to identify mutations in BRCA 1/2 genes in matched FFPE and blood samples

Autor:	Simon M. Hughes, Alexander Burton, Andrew Robb, Leif Schauser, Nathan Dennison, Bodil Oester, Adam Burke, Vishal Kapoor, Kyriakos Ttavas, Dietrich Lueerssen, Lea Thoegerson, Richard Dyson, Juergen Lauber
Rok vydání:	2018
Předmět:	Oncology Cancer Research medicine.medical_specialty endocrine system diseases business.industry Germline mutation Clinical evidence Internal medicine Medicine Familial breast cancer skin and connective tissue diseases business Gene
Zdroj:	Journal of Clinical Oncology. 36:e17536-e17536
ISSN:	1527-7755 0732-183X
Popis:	e17536Background: Supported by strong clinical evidence, testing for germline mutations in BRCA1 and BRCA2 in suspected familial breast cancer cases has gradually become common practice, especially...
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::9418a3f024bcbbd768eb450889c94b58 https://doi.org/10.1200/jco.2018.36.15_suppl.e17536 Zobrazit plný text záznamu