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.
Variants in KMT2A in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome. Genes 2024, 15, 211.
https://doi.org/10.3390/genes15020211
AMA Style
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
Chicago/Turabian Style
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
APA Style
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
