APA引文

T, K., I, V., M, S., S, S., J, K., G, B., & D, S. (2023, March). Keratitis-ichthyosis-deafness syndrome with heterozygous p.D50N in the GJB2 gene in two Serbian adult patients. Balkan Journal of Medical Genetics.

Chicago Style (17th ed.) Citation

T, Kalezić, Vuković I, Stojković M, Stanojlović S, Karanović J, Brajušković G, and Savić-Pavićević D. "Keratitis-ichthyosis-deafness Syndrome with Heterozygous P.D50N in the GJB2 Gene in Two Serbian Adult Patients." Balkan Journal of Medical Genetics Mar. 2023.

MLA引文

T, Kalezić, et al. "Keratitis-ichthyosis-deafness Syndrome with Heterozygous P.D50N in the GJB2 Gene in Two Serbian Adult Patients." Balkan Journal of Medical Genetics, Mar. 2023.