Yavaş, C. Et Al. 2022. Whole-Exome Sequencing (WES) results of 50 patients with chronic kidney diseases: a perspective of Alport syndrome. Revista da Associacao Medica Brasileira , vol.68, no.9 , 1282-1287.

Yavaş, C., Ün, C., Çelebi, E., Gezdirici, A., Doğan, M., İli, E. G., ... Doğan, T.(2022). Whole-Exome Sequencing (WES) results of 50 patients with chronic kidney diseases: a perspective of Alport syndrome. Revista da Associacao Medica Brasileira , vol.68, no.9, 1282-1287.

Yavaş, Cüneyd Et Al. "Whole-Exome Sequencing (WES) results of 50 patients with chronic kidney diseases: a perspective of Alport syndrome," Revista da Associacao Medica Brasileira , vol.68, no.9, 1282-1287, 2022

Yavaş, Cüneyd Et Al. "Whole-Exome Sequencing (WES) results of 50 patients with chronic kidney diseases: a perspective of Alport syndrome." Revista da Associacao Medica Brasileira , vol.68, no.9, pp.1282-1287, 2022

Yavaş, C. Et Al. (2022) . "Whole-Exome Sequencing (WES) results of 50 patients with chronic kidney diseases: a perspective of Alport syndrome." Revista da Associacao Medica Brasileira , vol.68, no.9, pp.1282-1287.

@article{article, author={Cüneyd Yavaş Et Al. }, title={Whole-Exome Sequencing (WES) results of 50 patients with chronic kidney diseases: a perspective of Alport syndrome}, journal={Revista da Associacao Medica Brasileira}, year=2022, pages={1282-1287} }