Wojcik, M. H., Lemire, G., Berger, E., Zaki, M. S., Wissmann, M., Win, W., . . . O’Donnell-Luria, A. (2024). Genome sequencing for diagnosing rare diseases. The New England journal of medicine, 390(21), . https://doi.org/10.1056/NEJMoa2314761
Chicago Style (17th ed.) CitationWojcik, Monica H., et al. "Genome Sequencing for Diagnosing Rare Diseases." The New England Journal of Medicine 390, no. 21 (2024). https://doi.org/10.1056/NEJMoa2314761.
MLA (9th ed.) CitationWojcik, Monica H., et al. "Genome Sequencing for Diagnosing Rare Diseases." The New England Journal of Medicine, vol. 390, no. 21, 2024, https://doi.org/10.1056/NEJMoa2314761.
Warning: These citations may not always be 100% accurate.