Human Genome Epidemiology Literature Finder
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Records 1 - 3 (of 3 Records) |
| Query Trace: Ovarian Neoplasms and RECQL[original query] |
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| Identification and Functional Testing of ERCC2 Mutations in a Multi-national Cohort of Patients with Familial Breast- and Ovarian Cancer. PLoS genetics 2016 Aug 12 (8): e1006248. Rump Andreas, Benet-Pages Anna, Schubert Steffen, Kuhlmann Jan Dominik, Janavi?ius Ram?nas, Machá?ková Eva, Foretová Lenka, Kleibl Zdenek, Lhota Filip, Zemankova Petra, Betcheva-Krajcir Elitza, Mackenroth Luisa, Hackmann Karl, Lehmann Janin, Nissen Anke, DiDonato Nataliya, Opitz Romy, Thiele Holger, Kast Karin, Wimberger Pauline, Holinski-Feder Elke, Emmert Steffen, Schröck Evelin, Klink Barba |
| FANCM and RECQL genetic variants and breast cancer susceptibility: relevance to South Poland and West Ukraine. BMC medical genetics 2018 1 19 (1): 12. Nguyen-Dumont Tú, Myszka Aleksander, Karpinski Pawel, Sasiadek Maria M, Akopyan Hayane, Hammet Fleur, Tsimiklis Helen, Park Daniel J, Pope Bernard J, Slezak Ryszard, Kitsera Nataliya, Siekierzynska Aleksandra, Southey Melissa |
| Variant Identification in BARD1, PRDM9, RCC1, and RECQL in Patients with Ovarian Cancer by Targeted Next-generation Sequencing of DNA Pools. Cancer prevention research (Philadelphia, Pa.) 2021 12 15 (3): 151-160. Suszynska Malwina, Ratajska Magdalena, Galka-Marciniak Paulina, Ryszkowska Aleksandra, Wydra Dariusz, Debniak Jaroslaw, Jasiak Anna, Wasag Bartosz, Cybulski Cezary, Kozlowski Pio |
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