Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders

MLA

Gregory Costain, et al. “Rare Copy Number Variations Affecting the Synaptic Gene DMXL2 in Neurodevelopmental Disorders.” Journal of Neurodevelopmental Disorders, vol. 11, no. 1, Feb. 2019, pp. 1–10. EBSCOhost, https://doi.org/10.1186/s11689-019-9263-3.

APA

Gregory Costain, Susan Walker, Bob Argiropoulos, Danielle A. Baribeau, Anne S. Bassett, Erik Boot, Koen Devriendt, Barbara Kellam, Christian R. Marshall, Aparna Prasad, Moises A. Serrano, D. James Stavropoulos, Hope Twede, Joris R. Vermeesch, Jacob A. S. Vorstman, & Stephen W. Scherer. (2019). Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders. Journal of Neurodevelopmental Disorders, 11(1), 1–10. https://doi.org/10.1186/s11689-019-9263-3

Chicago

Gregory Costain, Susan Walker, Bob Argiropoulos, Danielle A. Baribeau, Anne S. Bassett, Erik Boot, Koen Devriendt, et al. 2019. “Rare Copy Number Variations Affecting the Synaptic Gene DMXL2 in Neurodevelopmental Disorders.” Journal of Neurodevelopmental Disorders 11 (1): 1–10. doi:10.1186/s11689-019-9263-3.