APA (7th ed.) Citation

Cederquist, K., Emanuelsson, M., Wiklund, F., Golovleva, I., Palmqvist, R., & Grönberg, H. (2005). Two Swedish founder MSH6 mutations, one nonsense and one missense, conferring high cumulative risk of Lynch syndrome. Clinical Genetics, 68(6), 533. https://doi.org/10.1111/j.1399-0004.2005.00537.x

Chicago Style (17th ed.) Citation

Cederquist, K., M. Emanuelsson, F. Wiklund, I. Golovleva, R. Palmqvist, and H. Grönberg. "Two Swedish Founder MSH6 Mutations, One Nonsense and One Missense, Conferring High Cumulative Risk of Lynch Syndrome." Clinical Genetics 68, no. 6 (2005): 533. https://doi.org/10.1111/j.1399-0004.2005.00537.x.

MLA (9th ed.) Citation

Cederquist, K., et al. "Two Swedish Founder MSH6 Mutations, One Nonsense and One Missense, Conferring High Cumulative Risk of Lynch Syndrome." Clinical Genetics, vol. 68, no. 6, 2005, p. 533, https://doi.org/10.1111/j.1399-0004.2005.00537.x.