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• W2078045978 abstract "Although heritable factors are an important determinant of risk of early-onset cancer, the majority of these malignancies appear to occur sporadically without identifiable risk factors. Germline de novo copy-number variations (CNVs) have been observed in sporadic neurocognitive and cardiovascular disorders. We explored this mechanism in 382 genomes of 116 early-onset cancer case-parent trios and unaffected siblings. Unique de novo germline CNVs were not observed in 107 breast or colon cancer trios or controls but were indeed found in 7% of 43 testicular germ cell tumor trios; this percentage exceeds background CNV rates and suggests a rare de novo genetic paradigm for susceptibility to some human malignancies." @default.
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• W2078045978 date "2012-08-01" @default.
• W2078045978 modified "2023-10-14" @default.
• W2078045978 title "Rare De Novo Germline Copy-Number Variation in Testicular Cancer" @default.
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• W2078045978 doi "https://doi.org/10.1016/j.ajhg.2012.06.019" @default.
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