Rafi, S. K., & Butler, M. G. (2020). The 15q11.2 BP1-BP2 Microdeletion (Burnside–Butler) Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations with Neurodevelopmental Disorders. Int J Mol Sci.
Citação norma ChicagoRafi, Syed K., and Merlin G. Butler. "The 15q11.2 BP1-BP2 Microdeletion (Burnside–Butler) Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations With Neurodevelopmental Disorders." Int J Mol Sci 2020.
Citação norma MLARafi, Syed K., and Merlin G. Butler. "The 15q11.2 BP1-BP2 Microdeletion (Burnside–Butler) Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations With Neurodevelopmental Disorders." Int J Mol Sci 2020.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.