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Rare germline copy number variants (CNVs) and breast cancer risk.
Commun Biol. 2022 Jan 18;5(1):65. doi: 10.1038/s42003-021-02990-6.
Commun Biol. 2022.
PMID: 35042965
Free PMC article.
Association of recurrent mutations in BRCA1, BRCA2, RAD51C, PALB2, and CHEK2 with the risk of borderline ovarian tumor.
Ogrodniczak A, Menkiszak J, Gronwald J, Tomiczek-Szwiec J, Szwiec M, Cybulski C, Dębniak T, Huzarski T, Tołoczko-Grabarek A, Byrski T, Białkowska K, Prajzendanc K, Baszuk P, Lubiński J, Jakubowska A.
Ogrodniczak A, et al.
Hered Cancer Clin Pract. 2022 Mar 21;20(1):11. doi: 10.1186/s13053-022-00218-0.
Hered Cancer Clin Pract. 2022.
PMID: 35313928
Free PMC article.
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Genetic Aspects of Problematic and Risky Internet Use in Young Men-Analysis of ANKK1, DRD2 and NTRK3 Gene Polymorphism.
Rył A, Tomska N, Jakubowska A, Ogrodniczak A, Palma J, Rotter I.
Rył A, et al. Among authors: ogrodniczak a.
Genes (Basel). 2024 Jan 27;15(2):169. doi: 10.3390/genes15020169.
Genes (Basel). 2024.
PMID: 38397159
Free PMC article.
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