HuGE Literature Finder
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Records 1-2
Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromes.
Clinical endocrinology 2013 Dec 79 (6): 817-23. P?czkowska Mariola, Kowalska Aldona, Sygut Jacek, Waligórski Dariusz, Malinoc Angelica, Janaszek-Sitkowska Hanna, Prejbisz Aleksander, Januszewicz Andrzej, Neumann Hartmut P |
Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors.
Familial cancer 2012 Mar 11 (1): 19-26. Rahner Nils, Brockschmidt Felix F, Steinke Verena, Kahl Philip, Becker Tim, Vasen Hans F A, Wijnen Juul T, Tops Carli J M, Holinski-Feder Elke, Ligtenberg Marjolijn J L, Spruijt Liesbeth, Görgens Heike, Stemmler Susanne, Kloor Matthias, Dietmaier Wolfgang, , Schumacher Johannes, Nöthen Markus M, Propping Pet |
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