Article Versions Notes

Paduano F, Colao E, Loddo S, Orlando V, Trapasso F, Novelli A, Perrotti N, Iuliano R. 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. 2020; 11(5):525. https://doi.org/10.3390/genes11050525

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, no. 5: 525. https://doi.org/10.3390/genes11050525

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