Παραπομπή σε μορφή APA (7η εκδ.)

F, P., S, P., G, N., C, M., R, B., M, S., & FM, S. (2026). Further delineation of 2p13.2-p11.2 deletion syndrome by optical genome mapping. Neurogenetics, 27(1), . https://doi.org/10.1007/s10048-026-00942-y

Παραπομπή σε μορφή Chicago (17η εκδ.)

F, Privitera, Pagano S, Nutile G, Meossi C, Battini R, Schifino M, και Santorelli FM. "Further Delineation of 2p13.2-p11.2 Deletion Syndrome by Optical Genome Mapping." Neurogenetics 27, no. 1 (2026). https://doi.org/10.1007/s10048-026-00942-y.

Παραπομπή σε μορφή MLA (9th εκδ.)

F, Privitera, et al. "Further Delineation of 2p13.2-p11.2 Deletion Syndrome by Optical Genome Mapping." Neurogenetics, vol. 27, no. 1, 2026, https://doi.org/10.1007/s10048-026-00942-y.