Paduano, F., Colao, E., Loddo, S., Orlando, V., Trapasso, F., Novelli, A., . . . 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 (Basel).
シカゴスタイル引用形Paduano, Francesco, Emma Colao, Sara Loddo, Valeria Orlando, Francesco Trapasso, Antonio Novelli, Nicola Perrotti, , Rodolfo Iuliano. "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 (Basel) 2020.
MLA引用形式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 (Basel) 2020.