Cite
Mutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in human testis determination.
MLA
Pearlman, Alexander, et al. “Mutations in MAP3K1 Cause 46,XY Disorders of Sex Development and Implicate a Common Signal Transduction Pathway in Human Testis Determination.” American Journal of Human Genetics, vol. 87, no. 6, Dec. 2010, pp. 898–904. EBSCOhost, https://doi.org/10.1016/j.ajhg.2010.11.003.
APA
Pearlman, A., Loke, J., Le Caignec, C., White, S., Chin, L., Friedman, A., Warr, N., Willan, J., Brauer, D., Farmer, C., Brooks, E., Oddoux, C., Riley, B., Shajahan, S., Camerino, G., Homfray, T., Crosby, A. H., Couper, J., David, A., … Ostrer, H. (2010). Mutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in human testis determination. American Journal of Human Genetics, 87(6), 898–904. https://doi.org/10.1016/j.ajhg.2010.11.003
Chicago
Pearlman, Alexander, Johnny Loke, Cedric Le Caignec, Stefan White, Lisa Chin, Andrew Friedman, Nicholas Warr, et al. 2010. “Mutations in MAP3K1 Cause 46,XY Disorders of Sex Development and Implicate a Common Signal Transduction Pathway in Human Testis Determination.” American Journal of Human Genetics 87 (6): 898–904. doi:10.1016/j.ajhg.2010.11.003.