SAYGILI, S. K. Et Al. 2023. A novel homozygous missense variant in TBC1D31 in a consanguineous family with congenital anomalies of the kidney and urinary tract (CAKUT). Clinical Genetics , vol.104, no.6 , 679-685.

SAYGILI, S. K., KOŞUKCU, C., BAŞTUĞ, T., DOĞAN EKİCİ, A. I., YILMAZ, E. M., Kalyoncu, A. U., ... Ağbaş, A.(2023). A novel homozygous missense variant in TBC1D31 in a consanguineous family with congenital anomalies of the kidney and urinary tract (CAKUT). Clinical Genetics , vol.104, no.6, 679-685.

SAYGILI, Seha Et Al. "A novel homozygous missense variant in TBC1D31 in a consanguineous family with congenital anomalies of the kidney and urinary tract (CAKUT)," Clinical Genetics , vol.104, no.6, 679-685, 2023

SAYGILI, Seha K. Et Al. "A novel homozygous missense variant in TBC1D31 in a consanguineous family with congenital anomalies of the kidney and urinary tract (CAKUT)." Clinical Genetics , vol.104, no.6, pp.679-685, 2023

SAYGILI, S. K. Et Al. (2023) . "A novel homozygous missense variant in TBC1D31 in a consanguineous family with congenital anomalies of the kidney and urinary tract (CAKUT)." Clinical Genetics , vol.104, no.6, pp.679-685.

@article{article, author={Seha Kamil SAYGILI Et Al. }, title={A novel homozygous missense variant in TBC1D31 in a consanguineous family with congenital anomalies of the kidney and urinary tract (CAKUT)}, journal={Clinical Genetics}, year=2023, pages={679-685} }