Saygili, S. Et Al. 2020. A homozygousHOXA11variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract. CLINICAL GENETICS , vol.98, no.4 , 390-395.

Saygili, S., Atayar, E., Canpolat, N., ELİÇEVİK, M., KURUĞOĞLU, S., Sever, L., ... Caliskan, S.(2020). A homozygousHOXA11variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract. CLINICAL GENETICS , vol.98, no.4, 390-395.

Saygili, Seha Et Al. "A homozygousHOXA11variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract," CLINICAL GENETICS , vol.98, no.4, 390-395, 2020

Saygili, Seha Et Al. "A homozygousHOXA11variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract." CLINICAL GENETICS , vol.98, no.4, pp.390-395, 2020

Saygili, S. Et Al. (2020) . "A homozygousHOXA11variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract." CLINICAL GENETICS , vol.98, no.4, pp.390-395.

@article{article, author={Seha Saygili Et Al. }, title={A homozygousHOXA11variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract}, journal={CLINICAL GENETICS}, year=2020, pages={390-395} }