Cite
A homozygous HOXA11 variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract.
MLA
Saygili, Seha, et al. “A Homozygous HOXA11 Variation as a Potential Novel Cause of Autosomal Recessive Congenital Anomalies of the Kidney and Urinary Tract.” Clinical Genetics, vol. 98, no. 4, Oct. 2020, pp. 390–95. EBSCOhost, https://doi.org/10.1111/cge.13813.
APA
Saygili, S., Atayar, E., Canpolat, N., Elicevik, M., Kurugoglu, S., Sever, L., Caliskan, S., & Ozaltin, F. (2020). A homozygous HOXA11 variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract. Clinical Genetics, 98(4), 390–395. https://doi.org/10.1111/cge.13813
Chicago
Saygili, Seha, Emine Atayar, Nur Canpolat, Mehmet Elicevik, Sebuh Kurugoglu, Lale Sever, Salim Caliskan, and Fatih Ozaltin. 2020. “A Homozygous HOXA11 Variation as a Potential Novel Cause of Autosomal Recessive Congenital Anomalies of the Kidney and Urinary Tract.” Clinical Genetics 98 (4): 390–95. doi:10.1111/cge.13813.