Vesico-Ureteral Reflux

Displaying 1 - 2 of 2CSV
Riedhammer, K. M., Nguyen, T.-M. T., Koşukcu, C., Calzada-Wack, J., Li, Y., Assia Batzir, N., Saygılı, S., Wimmers, V., Kim, G.-J., Chrysanthou, M., Bakey, Z., Sofrin-Drucker, E., Kraiger, M., Sanz-Moreno, A., Amarie, O. V., Rathkolb, B., Klein-Rodewald, T., Garrett, L., Hölter, S. M., … Hoefele, J. (2024). Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT). Kidney International, 105(4), 844–864. https://doi.org/10.1016/j.kint.2023.11.032
Publication Date
Ahram, D. F., Lim, T. Y., Ke, J., Jin, G., Verbitsky, M., Bodria, M., Kil, B. H., Chatterjee, D., Piva, S. E., Marasa, M., Zhang, J. Y., Cocchi, E., Caridi, G., Gucev, Z., Lozanovski, V. J., Pisani, I., Izzi, C., Savoldi, G., Gnutti, B., … Sanna-Cherchi, S. (2023). Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis. Journal of the American Society of Nephrology, 34(6), 1105–1119. https://doi.org/10.1681/asn.0000000000000132
Publication Date