Sotirova, V. Et Al. 1999. Molecular genetic study of families with pseudoexfoliation syndrome (PEX) suggests two putative locations on 2p14-2Cen and 2q35-q36 regions. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE , vol.40, no.4 .

Sotirova, V., Irkec, M., PERÇİN, F. E., Bladow, K., Damji, K., & Sarfarazi, M., (1999). Molecular genetic study of families with pseudoexfoliation syndrome (PEX) suggests two putative locations on 2p14-2Cen and 2q35-q36 regions. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE , vol.40, no.4.

Sotirova, V Et Al. "Molecular genetic study of families with pseudoexfoliation syndrome (PEX) suggests two putative locations on 2p14-2Cen and 2q35-q36 regions," INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE , vol.40, no.4, 1999

Sotirova, V Et Al. "Molecular genetic study of families with pseudoexfoliation syndrome (PEX) suggests two putative locations on 2p14-2Cen and 2q35-q36 regions." INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE , vol.40, no.4, 1999

Sotirova, V. Et Al. (1999) . "Molecular genetic study of families with pseudoexfoliation syndrome (PEX) suggests two putative locations on 2p14-2Cen and 2q35-q36 regions." INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE , vol.40, no.4.

@article{article, author={V Sotirova Et Al. }, title={Molecular genetic study of families with pseudoexfoliation syndrome (PEX) suggests two putative locations on 2p14-2Cen and 2q35-q36 regions}, journal={INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE}, year=1999}