APA (7th ed.) Citation

PB, C., CA, S., SJ, S., J, L., MT, M., AG, E., . . . AL, B. (2011). Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE. Human molecular genetics, 20(22), 4360. https://doi.org/10.1093/hmg/ddr363

Chicago Style (17th ed.) Citation

PB, Celestino-Soper, et al. "Use of Array CGH to Detect Exonic Copy Number Variants Throughout the Genome in Autism Families Detects a Novel Deletion in TMLHE." Human Molecular Genetics 20, no. 22 (2011): 4360. https://doi.org/10.1093/hmg/ddr363.

MLA (9th ed.) Citation

PB, Celestino-Soper, et al. "Use of Array CGH to Detect Exonic Copy Number Variants Throughout the Genome in Autism Families Detects a Novel Deletion in TMLHE." Human Molecular Genetics, vol. 20, no. 22, 2011, p. 4360, https://doi.org/10.1093/hmg/ddr363.