APA (7th ed.) Citation

F, S., A, L., É, P., I, K., K, N., T, A., . . . I, H. (2026). Phenocopies of 22q11.2DS: Revealing genetic diversity in clinically suspected 22q11.2 deletion syndrome. Molecular and cellular pediatrics, 13(1), . https://doi.org/10.1186/s40348-026-00236-1

Chicago Style (17th ed.) Citation

F, Szumutku, et al. "Phenocopies of 22q11.2DS: Revealing Genetic Diversity in Clinically Suspected 22q11.2 Deletion Syndrome." Molecular and Cellular Pediatrics 13, no. 1 (2026). https://doi.org/10.1186/s40348-026-00236-1.

MLA (9th ed.) Citation

F, Szumutku, et al. "Phenocopies of 22q11.2DS: Revealing Genetic Diversity in Clinically Suspected 22q11.2 Deletion Syndrome." Molecular and Cellular Pediatrics, vol. 13, no. 1, 2026, https://doi.org/10.1186/s40348-026-00236-1.