APA (7th ed.) Citation

Pagnamenta, A. T., Khan, H., Walker, S., Gerrelli, D., Wing, K., Bonaglia, M. C., . . . Monaco, A. P. (2011). Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability. Journal of medical genetics, 48(1), 48-54. https://doi.org/10.1136/jmg.2010.079426

Chicago Style (17th ed.) Citation

Pagnamenta, Alistair T., et al. "Rare Familial 16q21 Microdeletions Under a Linkage Peak Implicate Cadherin 8 (CDH8) in Susceptibility to Autism and Learning Disability." Journal of Medical Genetics 48, no. 1 (2011): 48-54. https://doi.org/10.1136/jmg.2010.079426.

MLA (9th ed.) Citation

Pagnamenta, Alistair T., et al. "Rare Familial 16q21 Microdeletions Under a Linkage Peak Implicate Cadherin 8 (CDH8) in Susceptibility to Autism and Learning Disability." Journal of Medical Genetics, vol. 48, no. 1, 2011, pp. 48-54, https://doi.org/10.1136/jmg.2010.079426.