Turro, E., Astle, W., Megy, K., Bennett, D., Ormondroyd, E., Roberts, I., . . . NIHR BioResource for the 100,000 Genomes Project. (2020). Whole-genome sequencing of patients with rare diseases in a national health system. Springer Nature.
Chicago Style (17th ed.) CitationTurro, E., et al. Whole-genome Sequencing of Patients with Rare Diseases in a National Health System. Springer Nature, 2020.
MLA引文Turro, E., et al. Whole-genome Sequencing of Patients with Rare Diseases in a National Health System. Springer Nature, 2020.
警告:這些引文格式不一定是100%准確.