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Silveira HG, Steiner CE, Toccoli G, Angeloni LL, Heleno JL, Spineli-Silva S, dos Santos AM, Vieira TP, Melaragno MI, Gil-da-Silva-Lopes VL. Variants in KMT2A in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome. Genes. 2024; 15(2):211. https://doi.org/10.3390/genes15020211

Silveira, Henrique Garcia, Carlos Eduardo Steiner, Giovana Toccoli, Luise Longo Angeloni, Júlia Lôndero Heleno, Samira Spineli-Silva, Ana Mondadori dos Santos, Társis Paiva Vieira, Maria Isabel Melaragno, and Vera Lúcia Gil-da-Silva-Lopes. 2024. "Variants in KMT2A in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome" Genes 15, no. 2: 211. https://doi.org/10.3390/genes15020211

Silveira, H. G., Steiner, C. E., Toccoli, G., Angeloni, L. L., Heleno, J. L., Spineli-Silva, S., dos Santos, A. M., Vieira, T. P., Melaragno, M. I., & Gil-da-Silva-Lopes, V. L. (2024). Variants in KMT2A in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome. Genes, 15(2), 211. https://doi.org/10.3390/genes15020211