A novel SRY gene mutation c.266 A>T (p.E89V) in a 46,XY complete gonadal dysgenesis patient.

MLA

Raveendran, Suresh Kumar, et al. “A Novel SRY Gene Mutation c.266 A>T (p.E89V) in a 46,XY Complete Gonadal Dysgenesis Patient.” Andrologia, vol. 51, no. 9, Oct. 2019, p. N.PAG. EBSCOhost, https://doi.org/10.1111/and.13377.

APA

Raveendran, S. K., Ramachandran, L., Joseph, L., Asokan, A. K., Raj, S., George, A., & James, J. (2019). A novel SRY gene mutation c.266 A>T (p.E89V) in a 46,XY complete gonadal dysgenesis patient. Andrologia, 51(9), N.PAG. https://doi.org/10.1111/and.13377

Chicago

Raveendran, Suresh Kumar, Lola Ramachandran, Lincy Joseph, Aneesh Kumar Asokan, Soumya Raj, Alex George, and Jimcy James. 2019. “A Novel SRY Gene Mutation c.266 A>T (p.E89V) in a 46,XY Complete Gonadal Dysgenesis Patient.” Andrologia 51 (9): N.PAG. doi:10.1111/and.13377.