APA (7th ed.) Citation

de Ligt, J., Boone, P. M., Pfundt, R., Vissers, L. E., Richmond, T., Geoghegan, J., . . . Hehir-Kwa, J. Y. (2013). Detection of Clinically Relevant Copy Number Variants with Whole-Exome Sequencing. Human mutation, 34(10), 1439-1448. https://doi.org/10.1002/humu.22387

Chicago Style (17th ed.) Citation

de Ligt, Joep, et al. "Detection of Clinically Relevant Copy Number Variants with Whole-Exome Sequencing." Human Mutation 34, no. 10 (2013): 1439-1448. https://doi.org/10.1002/humu.22387.

MLA (9th ed.) Citation

de Ligt, Joep, et al. "Detection of Clinically Relevant Copy Number Variants with Whole-Exome Sequencing." Human Mutation, vol. 34, no. 10, 2013, pp. 1439-1448, https://doi.org/10.1002/humu.22387.