APA način citiranja

van der Ven, A. T., Connaughton, D. M., Ityel, H., Mann, N., Nakayama, M., Chen, J., . . . Hildebrandt, F. (2018). Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract. J Am Soc Nephrol.

Čikaški stil citiranja

van der Ven, Amelie T., et al. "Whole-Exome Sequencing Identifies Causative Mutations in Families With Congenital Anomalies of the Kidney and Urinary Tract." J Am Soc Nephrol 2018.

MLA način citiranja

van der Ven, Amelie T., et al. "Whole-Exome Sequencing Identifies Causative Mutations in Families With Congenital Anomalies of the Kidney and Urinary Tract." J Am Soc Nephrol 2018.