APA (7th ed.) Citation

S, R., DP, K., T, S., K, R., B, M., & M, B. (2001). Recurrent mutations in the deafness gene GJB2 (connexin 26) in British Asian families. Journal of medical genetics, 38(8), 530. https://doi.org/10.1136/jmg.38.8.530

Chicago Style (17th ed.) Citation

S, Rickard, Kelsell DP, Sirimana T, Rajput K, MacArdle B, and Bitner-Glindzicz M. "Recurrent Mutations in the Deafness Gene GJB2 (connexin 26) in British Asian Families." Journal of Medical Genetics 38, no. 8 (2001): 530. https://doi.org/10.1136/jmg.38.8.530.

MLA (9th ed.) Citation

S, Rickard, et al. "Recurrent Mutations in the Deafness Gene GJB2 (connexin 26) in British Asian Families." Journal of Medical Genetics, vol. 38, no. 8, 2001, p. 530, https://doi.org/10.1136/jmg.38.8.530.