APA

Brooke A. M., Taylor N. F., Shepherd J. H., Gore M. E., Ahmad T., Lin L., Rumsby G., Papari-Zareei M., Auchus R. J., Achermann J. C. & Monson J. P. (20060629). A novel point mutation in P450c17 (CYP17) causing combined 17alpha-hydroxylase/17,20-lyase deficiency. : The Journal of clinical endocrinology and metabolism.

Chicago

Brooke A M, Taylor N F, Shepherd J H, Gore M E, Ahmad T, Lin L, Rumsby G, Papari-Zareei M, Auchus R J, Achermann J C and Monson J P. 20060629. A novel point mutation in P450c17 (CYP17) causing combined 17alpha-hydroxylase/17,20-lyase deficiency. : The Journal of clinical endocrinology and metabolism.

Harvard

Brooke A. M., Taylor N. F., Shepherd J. H., Gore M. E., Ahmad T., Lin L., Rumsby G., Papari-Zareei M., Auchus R. J., Achermann J. C. and Monson J. P. (20060629). A novel point mutation in P450c17 (CYP17) causing combined 17alpha-hydroxylase/17,20-lyase deficiency. : The Journal of clinical endocrinology and metabolism.

MLA

Brooke A M, Taylor N F, Shepherd J H, Gore M E, Ahmad T, Lin L, Rumsby G, Papari-Zareei M, Auchus R J, Achermann J C and Monson J P. A novel point mutation in P450c17 (CYP17) causing combined 17alpha-hydroxylase/17,20-lyase deficiency. : The Journal of clinical endocrinology and metabolism. 20060629.