APA (7th ed.) Citation

Watson, C. M., Holliday, D. L., Crinnion, L. A., & Bonthron, D. T. (2022). Long‐read nanopore DNA sequencing can resolve complex intragenic duplication/deletion variants, providing information to enable preimplantation genetic diagnosis. Prenatal diagnosis, 42(2), 226-232. https://doi.org/10.1002/pd.6089

Chicago Style (17th ed.) Citation

Watson, Christopher M., Deborah L. Holliday, Laura A. Crinnion, and David T. Bonthron. "Long‐read Nanopore DNA Sequencing Can Resolve Complex Intragenic Duplication/deletion Variants, Providing Information to Enable Preimplantation Genetic Diagnosis." Prenatal Diagnosis 42, no. 2 (2022): 226-232. https://doi.org/10.1002/pd.6089.

MLA (9th ed.) Citation

Watson, Christopher M., et al. "Long‐read Nanopore DNA Sequencing Can Resolve Complex Intragenic Duplication/deletion Variants, Providing Information to Enable Preimplantation Genetic Diagnosis." Prenatal Diagnosis, vol. 42, no. 2, 2022, pp. 226-232, https://doi.org/10.1002/pd.6089.