A, E., MA, F., M, P., & B, T. (2026). Phenotypic spectrum of 19p13.3 microdeletion: A fatal infant case with severe cardiomegaly and gastrointestinal manifestations. Molecular biology reports, 53(1), . https://doi.org/10.1007/s11033-026-12791-x
Παραπομπή σε μορφή Chicago (17η εκδ.)A, Eshghi, Fargi MA, Pandi M, και Tasharrofi B. "Phenotypic Spectrum of 19p13.3 Microdeletion: A Fatal Infant Case with Severe Cardiomegaly and Gastrointestinal Manifestations." Molecular Biology Reports 53, no. 1 (2026). https://doi.org/10.1007/s11033-026-12791-x.
Παραπομπή σε μορφή MLA (9th εκδ.)A, Eshghi, et al. "Phenotypic Spectrum of 19p13.3 Microdeletion: A Fatal Infant Case with Severe Cardiomegaly and Gastrointestinal Manifestations." Molecular Biology Reports, vol. 53, no. 1, 2026, https://doi.org/10.1007/s11033-026-12791-x.