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.
Citace podle Chicago (17th ed.)Turro, E., et al. Whole-genome Sequencing of Patients with Rare Diseases in a National Health System. Springer Nature, 2020.
Citace podle MLA (9th ed.)Turro, E., et al. Whole-genome Sequencing of Patients with Rare Diseases in a National Health System. Springer Nature, 2020.
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