Human Genome Epidemiology Literature Finder
|
Records 1 - 1 (of 1 Records) |
| Query Trace: Syndrome and PCNA[original query] |
|---|
| 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 |
- Page last reviewed:Feb 1, 2024
- Content source:

