Genome-wide analysis of common copy number variation and epithelial ovarian cancer risk

BACKGROUND: Germline DNA copy number variation (CNV) is a ubiquitous source of genetic variation and remains largely unexplored in association with epithelial ovarian cancer (EOC) risk. METHODS: CNV was quantified in the DNA of approximately 3500 cases and controls genotyped with the Illumina 610k a...

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Bibliografiset tiedot
Julkaisussa:Cancer Epidemiol Biomarkers Prev
Päätekijät: Reid, Brett M., Permuth, Jennifer B., Chen, Y. Ann, Fridley, Brooke L., Iversen, Edwin, Chen, Zhihua, Jim, Heather S., Vierkant, Robert A., Cunningham, Julie M., Barnholtz-Sloan, Jill, Narod, Steven, Risch, Harvey, Schildkraut, Joellen M., Goode, Ellen L., Monteiro, Alvaro N.A., Sellers, Thomas A.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2019
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6606353/
https://ncbi.nlm.nih.gov/pubmed/30948450
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1158/1055-9965.EPI-18-0833
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