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Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci
BACKGROUND: Known risk alleles for epithelial ovarian cancer (EOC) account for approximately 40% of the heritability for EOC. Copy number variants (CNVs) have not been investigated as EOC risk alleles in a large population cohort. METHODS: Single nucleotide polymorphism array data from 13 071 EOC ca...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949586/ https://www.ncbi.nlm.nih.gov/pubmed/36210504 http://dx.doi.org/10.1093/jnci/djac160 |