APA (7th ed.) Citation

HG, D., T, H., EM, P., AL, T., OJ, B., M, O., . . . KM, B. (2022). Genomics4RD: An integrated platform to share Canadian deep-phenotype and multiomic data for international rare disease gene discovery. Human mutation, 43(6), 800. https://doi.org/10.1002/humu.24354

Chicago Style (17th ed.) Citation

HG, Driver, et al. "Genomics4RD: An Integrated Platform to Share Canadian Deep-phenotype and Multiomic Data for International Rare Disease Gene Discovery." Human Mutation 43, no. 6 (2022): 800. https://doi.org/10.1002/humu.24354.

MLA (9th ed.) Citation

HG, Driver, et al. "Genomics4RD: An Integrated Platform to Share Canadian Deep-phenotype and Multiomic Data for International Rare Disease Gene Discovery." Human Mutation, vol. 43, no. 6, 2022, p. 800, https://doi.org/10.1002/humu.24354.