APA (7. basım) Alıntı

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 (17. basım) Atıf

Turro, E., et al. Whole-genome Sequencing of Patients with Rare Diseases in a National Health System. Springer Nature, 2020.

MLA (9th ed.) Atıf

Turro, E., et al. Whole-genome Sequencing of Patients with Rare Diseases in a National Health System. Springer Nature, 2020.