PERÇİN, F. E. Et Al. 2000. Human microphthalmia associated with mutations in the retinal homeobox gene CHX10. NATURE GENETICS , vol.25, no.4 , 397-401.

PERÇİN, F. E., Ploder, L., Yu, J., Arici, K., Horsford, D., Rutherford, A., ... Bapat, B.(2000). Human microphthalmia associated with mutations in the retinal homeobox gene CHX10. NATURE GENETICS , vol.25, no.4, 397-401.

PERÇİN, FERDA Et Al. "Human microphthalmia associated with mutations in the retinal homeobox gene CHX10," NATURE GENETICS , vol.25, no.4, 397-401, 2000

PERÇİN, FERDA E. Et Al. "Human microphthalmia associated with mutations in the retinal homeobox gene CHX10." NATURE GENETICS , vol.25, no.4, pp.397-401, 2000

PERÇİN, F. E. Et Al. (2000) . "Human microphthalmia associated with mutations in the retinal homeobox gene CHX10." NATURE GENETICS , vol.25, no.4, pp.397-401.

@article{article, author={FERDA EMRİYE PERÇİN Et Al. }, title={Human microphthalmia associated with mutations in the retinal homeobox gene CHX10}, journal={NATURE GENETICS}, year=2000, pages={397-401} }