APA (7th ed.) Citation

J, S., T, V., L, M., C, K., CM, S., D, Y., . . . M, G. (2017). Mutations in KIAA0753 cause Joubert syndrome associated with growth hormone deficiency. Human genetics, 136(4), 399. https://doi.org/10.1007/s00439-017-1765-z

Chicago Style (17th ed.) Citation

J, Stephen, et al. "Mutations in KIAA0753 Cause Joubert Syndrome Associated with Growth Hormone Deficiency." Human Genetics 136, no. 4 (2017): 399. https://doi.org/10.1007/s00439-017-1765-z.

MLA (9th ed.) Citation

J, Stephen, et al. "Mutations in KIAA0753 Cause Joubert Syndrome Associated with Growth Hormone Deficiency." Human Genetics, vol. 136, no. 4, 2017, p. 399, https://doi.org/10.1007/s00439-017-1765-z.