APA (7th ed.) Citation

Sanchis-Juan, A., Stephens, J., French, C. E., Gleadall, N., Mégy, K., Penkett, C., . . . Carss, K. J. (2018). Complex structural variants in Mendelian disorders: Identification and breakpoint resolution using short- and long-read genome sequencing. Genome medicine, 10(1), 95-10. https://doi.org/10.1186/s13073-018-0606-6

Chicago Style (17th ed.) Citation

Sanchis-Juan, Alba, et al. "Complex Structural Variants in Mendelian Disorders: Identification and Breakpoint Resolution Using Short- and Long-read Genome Sequencing." Genome Medicine 10, no. 1 (2018): 95-10. https://doi.org/10.1186/s13073-018-0606-6.

MLA (9th ed.) Citation

Sanchis-Juan, Alba, et al. "Complex Structural Variants in Mendelian Disorders: Identification and Breakpoint Resolution Using Short- and Long-read Genome Sequencing." Genome Medicine, vol. 10, no. 1, 2018, pp. 95-10, https://doi.org/10.1186/s13073-018-0606-6.