Kayser, K., Knebel Doeberitz, M. v., & Bork, P. (2018). Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes. International journal of cancer, 143(11), . https://doi.org/10.1002/ijc.31725
Chicago Style (17th ed.) CitationKayser, Katrin, Magnus von Knebel Doeberitz, and Peer Bork. "Copy Number Variation Analysis and Targeted NGS in 77 Families with Suspected Lynch Syndrome Reveals Novel Potential Causative Genes." International Journal of Cancer 143, no. 11 (2018). https://doi.org/10.1002/ijc.31725.
MLA (9th ed.) CitationKayser, Katrin, et al. "Copy Number Variation Analysis and Targeted NGS in 77 Families with Suspected Lynch Syndrome Reveals Novel Potential Causative Genes." International Journal of Cancer, vol. 143, no. 11, 2018, https://doi.org/10.1002/ijc.31725.