APA (7th ed.) Citation

Zhou, W., Li, Y., Zheng, H., He, M., Zhang, M., Chen, Q., . . . Zhang, X. (2025). Whole exome sequencing enhances diagnosis of hereditary bronchiectasis. Orphanet Journal of Rare Diseases, 20(1), 1. https://doi.org/10.1186/s13023-025-03661-z

Chicago Style (17th ed.) Citation

Zhou, Wangji, et al. "Whole Exome Sequencing Enhances Diagnosis of Hereditary Bronchiectasis." Orphanet Journal of Rare Diseases 20, no. 1 (2025): 1. https://doi.org/10.1186/s13023-025-03661-z.

MLA (9th ed.) Citation

Zhou, Wangji, et al. "Whole Exome Sequencing Enhances Diagnosis of Hereditary Bronchiectasis." Orphanet Journal of Rare Diseases, vol. 20, no. 1, 2025, p. 1, https://doi.org/10.1186/s13023-025-03661-z.