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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Bibliografiset tiedot
Päätekijät: Stadler, Zsofia K., Esposito, Diane, Shah, Sohela, Vijai, Joseph, Yamrom, Boris, Levy, Dan, Lee, Yoon-ha, Kendall, Jude, Leotta, Anthony, Ronemus, Michael, Hansen, Nichole, Sarrel, Kara, Rau-Murthy, Rohini, Schrader, Kasmintan, Kauff, Noah, Klein, Robert J., Lipkin, Steven M., Murali, Rajmohan, Robson, Mark, Sheinfeld, Joel, Feldman, Darren, Bosl, George, Norton, Larry, Wigler, Michael, Offit, Kenneth
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Elsevier 2012
Aiheet:
Report
Linkit: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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