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Autor:
Youlia M. Kirova, Piotr J. Wysocki, Judy W. C. Ho, Ute Hamann, Dominique Stoppa-Lyonnet, Fernando Schmitt, Gulnur Guler, Zheng Shu, Neva E. Haites, Peter Simmonds, Cornelis J.M. Lips, Janis Gardovskis, Alain Fourquet, Evangelia Razis, Jean-Yves Pierga, Johannes W. B. de Groot, Siniša Radulović, Kay Huebner, Diana Eccles, Lidia Larizza, Åke Borg, Niklas Loman, Thangarajan Rajkumar, Peter T. Silberstein, Rita K. Schmutzler, Arvids Irmejs, Håkan Olsson, Rolf H. Sijmons, Lenka Foretova, Evgeny N. Imyanitov, Winette T. A. van der Graaf, Henry T. Lynch, Pål Møller, Pax H.B. Willemse, Pavel Elsakov, Vladimir Zajac, Jae-Gahb Park, Jacob Smeltzer, Walter P. Weber, P. Goetz, Mira Brankovic-Magic, Marianna Bitina, Gunta Purkalne, Andris Gardovskis, Drakoulis Yannoukakos
Publikováno v:
Hereditary Cancer in Clinical Practice
Hereditary cancer in clinical practice, 5(3), 119-143. BioMed Central Ltd.
Hereditary cancer in clinical practice, 5(3), 119-143. BioMed Central Ltd.
BRCA1-associated cancers differ from non-hereditary cancers for many factors, including somatic mutation. It can be a subject of discussion that the natural history and response to treatment also may differ between the hereditary and sporadic subgrou