Panagiotou, E. S. Et Al. 2022. Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia. MOLECULAR VISION , vol.28 , 57-69.

Panagiotou, E. S., Fernandez-Fuentes, N., Farraj, L. A., McKibbin, M., ELÇİOĞLU, H. N., Jafri, H., ... ÇERMAN, E.(2022). Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia. MOLECULAR VISION , vol.28, 57-69.

Panagiotou, Evangelia Et Al. "Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia," MOLECULAR VISION , vol.28, 57-69, 2022

Panagiotou, Evangelia S. Et Al. "Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia." MOLECULAR VISION , vol.28, pp.57-69, 2022

Panagiotou, E. S. Et Al. (2022) . "Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia." MOLECULAR VISION , vol.28, pp.57-69.

@article{article, author={Evangelia S. Panagiotou Et Al. }, title={Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia}, journal={MOLECULAR VISION}, year=2022, pages={57-69} }