APA aipamena

Shirakawa, T., Nakashima, Y., Watanabe, S., Harada, S., Kinoshita, M., Kihara, T., . . . Dateki, S. (2018). A novel heterozygous GLI2 mutation in a patient with congenital urethral stricture and renal hypoplasia/dysplasia leading to end-stage renal failure. CEN Case Rep.

Chicago Style aipamena

Shirakawa, Toshihiko, et al. "A Novel Heterozygous GLI2 Mutation in a Patient With Congenital Urethral Stricture and Renal Hypoplasia/dysplasia Leading to End-stage Renal Failure." CEN Case Rep 2018.

MLA aipamena

Shirakawa, Toshihiko, et al. "A Novel Heterozygous GLI2 Mutation in a Patient With Congenital Urethral Stricture and Renal Hypoplasia/dysplasia Leading to End-stage Renal Failure." CEN Case Rep 2018.