Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT).


Riedhammer K. M., Nguyen T. T., Koşukcu C., Calzada-Wack J., Li Y., Saygılı S., ...Daha Fazla

medRxiv : the preprint server for health sciences, 2023 (Hakemli Dergi) identifier