Riedhammer, K. M. Et Al. 2024. Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT). Kidney International , vol.105, no.4 , 844-864.

Riedhammer, K. M., Nguyen, T. T., KOŞUKCU, C., Calzada-Wack, J., Li, Y., Assia Batzir, N., ... SAYGILI, S. K.(2024). Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT). Kidney International , vol.105, no.4, 844-864.

Riedhammer, Korbinian Et Al. "Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)," Kidney International , vol.105, no.4, 844-864, 2024

Riedhammer, Korbinian M. Et Al. "Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)." Kidney International , vol.105, no.4, pp.844-864, 2024

Riedhammer, K. M. Et Al. (2024) . "Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)." Kidney International , vol.105, no.4, pp.844-864.

@article{article, author={Korbinian M. Riedhammer Et Al. }, title={Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)}, journal={Kidney International}, year=2024, pages={844-864} }