Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study.

MLA

Peter, Michelle, et al. “Participant Experiences of Genome Sequencing for Rare Diseases in the 100,000 Genomes Project: A Mixed Methods Study.” European Journal of Human Genetics : EJHG, vol. 30, no. 5, May 2022, pp. 604–10. EBSCOhost, https://doi.org/10.1038/s41431-022-01065-2.

APA

Peter, M., Hammond, J., Sanderson, S. C., Gurasashvili, J., Hunter, A., Searle, B., Patch, C., Chitty, L. S., Hill, M., & Lewis, C. (2022). Participant experiences of genome sequencing for rare diseases in the 100,000 Genomes Project: a mixed methods study. European Journal of Human Genetics : EJHG, 30(5), 604–610. https://doi.org/10.1038/s41431-022-01065-2

Chicago

Peter, Michelle, Jennifer Hammond, Saskia C Sanderson, Jana Gurasashvili, Amy Hunter, Beverly Searle, Christine Patch, Lyn S Chitty, Melissa Hill, and Celine Lewis. 2022. “Participant Experiences of Genome Sequencing for Rare Diseases in the 100,000 Genomes Project: A Mixed Methods Study.” European Journal of Human Genetics : EJHG 30 (5): 604–10. doi:10.1038/s41431-022-01065-2.