M. Turaçli

A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region.

M. Sarfarazi, M. Barsoum-Homsy, L. Chevrette, 1996, Human molecular genetics.

Assignment of a locus (GLC3A) for primary congenital glaucoma (Buphthalmos) to 2p21 and evidence for genetic heterogeneity.

M. Sarfarazi, N. Akarsu, M. Barsoum-Homsy, 1995, Genomics.

Choroidal and Ganglion Cell Complex Thicknesses in Subjects with Type A Behavior Pattern: An Optical Coherence Tomography Study

A. Gül, M. Turaçli, A. Şengün, 2016 .

Sensorineural hearing loss in pseudoexfoliation.

M. Turaçli, O. Tekeli, M. Gerçeker, 2007, Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.

Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1.

A. Child, G. Brice, M. Sarfarazi, 1998, American journal of human genetics.

Exclusion of primary congenital glaucoma (buphthalmos) from two candidate regions of chromosome arm 6p and chromosome 11.

M. Sarfarazi, M. Barsoum-Homsy, L. Chevrette, 1996, American journal of medical genetics.