E. SUSAM Et Al. , "Brittle cornea syndrome with a novel pathogenic variant of PRDM5 gene," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, pp.119-120, 2022
SUSAM, E. Et Al. 2022. Brittle cornea syndrome with a novel pathogenic variant of PRDM5 gene. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1 , 119-120.
SUSAM, E., YILDIRIM, N., KOCAGİL, S., & ÇİLİNGİR, O., (2022). Brittle cornea syndrome with a novel pathogenic variant of PRDM5 gene. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, 119-120.
SUSAM, EZGİ Et Al. "Brittle cornea syndrome with a novel pathogenic variant of PRDM5 gene," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, 119-120, 2022
SUSAM, EZGİ Et Al. "Brittle cornea syndrome with a novel pathogenic variant of PRDM5 gene." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, pp.119-120, 2022
SUSAM, E. Et Al. (2022) . "Brittle cornea syndrome with a novel pathogenic variant of PRDM5 gene." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, pp.119-120.
@article{article, author={EZGİ SUSAM Et Al. }, title={Brittle cornea syndrome with a novel pathogenic variant of PRDM5 gene}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2022, pages={119-120} }