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., Kosukcu, C., BAŞTUĞ, T., AKGÜN DOĞAN, Ö., Yilmaz, E. K., 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 KAMİL 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} }