Cite
7q35 Microdeletion and 15q13.3 and Xp22.33 Microduplications in a Patient with Severe Myoclonic Epilepsy, Microcephaly, Dysmorphisms, Severe Psychomotor Delay and Intellectual Disability.
MLA
Paduano, Francesco, et al. “7q35 Microdeletion and 15q13.3 and Xp22.33 Microduplications in a Patient with Severe Myoclonic Epilepsy, Microcephaly, Dysmorphisms, Severe Psychomotor Delay and Intellectual Disability.” Genes, vol. 11, no. 5, May 2020, p. 525. EBSCOhost, https://doi.org/10.3390/genes11050525.
APA
Paduano, F., Colao, E., Loddo, S., Orlando, V., Trapasso, F., Novelli, A., Perrotti, N., & Iuliano, R. (2020). 7q35 Microdeletion and 15q13.3 and Xp22.33 Microduplications in a Patient with Severe Myoclonic Epilepsy, Microcephaly, Dysmorphisms, Severe Psychomotor Delay and Intellectual Disability. Genes, 11(5), 525. https://doi.org/10.3390/genes11050525
Chicago
Paduano, Francesco, Emma Colao, Sara Loddo, Valeria Orlando, Francesco Trapasso, Antonio Novelli, Nicola Perrotti, and Rodolfo Iuliano. 2020. “7q35 Microdeletion and 15q13.3 and Xp22.33 Microduplications in a Patient with Severe Myoclonic Epilepsy, Microcephaly, Dysmorphisms, Severe Psychomotor Delay and Intellectual Disability.” Genes 11 (5): 525. doi:10.3390/genes11050525.