APA引文

Kurtas, N., Arrigoni, F., Errichiello, E., Zucca, C., Maghini, C., D’Angelo, M. G., . . . Bonaglia, M. C. (2018). Chromothripsis and ring chromosome 22: A paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome). J Med Genet.

Citação norma Chicago

Kurtas, Nehir, et al. "Chromothripsis and Ring Chromosome 22: A Paradigm of Genomic Complexity in the Phelan-McDermid Syndrome (22q13 Deletion Syndrome)." J Med Genet 2018.

MLA引文

Kurtas, Nehir, et al. "Chromothripsis and Ring Chromosome 22: A Paradigm of Genomic Complexity in the Phelan-McDermid Syndrome (22q13 Deletion Syndrome)." J Med Genet 2018.