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Rare De Novo Germline Copy-Number Variation in Testicular Cancer
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 di...
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , |
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格式: | Artigo |
語言: | Inglês |
出版: |
Elsevier
2012
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主題: | |
在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3415553/ https://ncbi.nlm.nih.gov/pubmed/22863192 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2012.06.019 |
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