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.
Chicago Style aipamenaRafi, 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.
MLA aipamenaRafi, 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.
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