TEMEL, Ş. G. Et Al. 2020. Unique combination and in silico modeling of biallelic POLR3A variants as a cause of Wiedemann-Rautenstrauch syndrome. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.12 , 1675-1680.

TEMEL, Ş. G., Ergoren, M. C., Manara, E., Paolacci, S., Tuncel, G., Gul, S., ... Bertelli, M.(2020). Unique combination and in silico modeling of biallelic POLR3A variants as a cause of Wiedemann-Rautenstrauch syndrome. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.12, 1675-1680.

TEMEL, ŞEHİME Et Al. "Unique combination and in silico modeling of biallelic POLR3A variants as a cause of Wiedemann-Rautenstrauch syndrome," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.12, 1675-1680, 2020

TEMEL, ŞEHİME G. Et Al. "Unique combination and in silico modeling of biallelic POLR3A variants as a cause of Wiedemann-Rautenstrauch syndrome." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.12, pp.1675-1680, 2020

TEMEL, Ş. G. Et Al. (2020) . "Unique combination and in silico modeling of biallelic POLR3A variants as a cause of Wiedemann-Rautenstrauch syndrome." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.28, no.12, pp.1675-1680.

@article{article, author={ŞEHİME GÜLSÜN TEMEL Et Al. }, title={Unique combination and in silico modeling of biallelic POLR3A variants as a cause of Wiedemann-Rautenstrauch syndrome}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2020, pages={1675-1680} }