REFERENCES
- MacKinnon J R, Giubilato A F, et al. Primary infantile glaucoma in an Australian population. Clin Experiment Ophthalmol 2004; 32: 14–8
- Gencik A F, Gencikova A F, Ferak V. Population genetical aspects of primary congenital glaucoma. I. Incidence, prevalence, gene frequency, and age of onset. Hum Genet. 1982; 61: 193–7
- Dandona L F, Williams J D, Williams B C, et al. Population-based assessment of childhood blindness in southern India. Arch Ophthalmol. 1998; 116: 545–6
- Maumenee A E. The pathogenesis of congenital glaucoma; a new theory. Am J Ophthalmol. 1959; 47: 827–58
- Gorin G. Developmental Glaucoma. A concept based on correlation of gonioscopic findings with clinical manifestations. Am J Ophthalmol 1964; 58: 572–80
- Kimura R F, Levene R Z. Gonioscopic differences between eyes with primary open-angle glaucoma and normal eyes in subjects over the age of forty. Trans Am Ophthalmol Soc. 975; 73: 74–85
- Lichter P R. Iris processes in 340 eyes. Am J Ophthalmol. 1969; 68: 872–8
- Cohn A C, Kearns L S, Savarirayan R F, et al. Chromosomal abnormalities and glaucoma: A case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pter. Ophthalmic Genet. 2005; 26: 45–53
- Weisschuh N F, Schiefer U. Progress in the genetics of glaucoma. Dev Ophthalmol. 2003; 37: 83–93
- Ray K F, Mukhopadhyay A F, Acharya M. Recent advances in molecular genetics of glaucoma. Mol Cell Biochem. 2003; 253: 223–31
- Kaur K F, Reddy A B, Mukhopadhyay A F, et al. Myocilin gene implicated in primary congenital glaucoma. Clin Genet 2005; 67: 335–40
- Ho C L, Walton D S. Primary congenital glaucoma: 2004 update. J Pediatr Ophthalmol Strabismus 2004; 41: 271–88
- Demenais F F, Elston R C, Bonaiti C F, et al. Segregation analysis of congenital glaucoma: approach by two differential models. Am J Hum Genet. 1981; 33: 300–6
- Bonaiti C F, Demenais F F, Briard M L, et al. Consanguinity in multifactorial inheritance. Application to data on congenital glaucoma. Hum Hered 1978; 28: 361–71
- Bejjani B A, Xu L F, Armstrong D F, et al. Expression patterns of cytochrome P4501B1 (Cyp1b1) in FVB/N mouse eyes. Exp Eye Res. 2002; 75: 249–57
- Sarfarazi M F, Stoilov I F, Schenkman J B. Genetics and biochemistry of primary congenital glaucoma. Ophthalmol Clin North Am 2003; 16: 543–54
- Panicker S G, Reddy A B, Mandal A K, et al. Identification of novel mutations causing familial primary congenital glaucoma in Indian pedigrees. Invest Ophthalmol Vis Sci 2002; 43: 1358–66
- Panicker S G, Mandal A K, Reddy A B, et al. Correlations of genotype with phenotype in Indian patients with primary congenital glaucoma. Invest Ophthalmol Vis Sci. 2004; 45: 1149–56
- Pollack A F, Oliver M. Congenital glaucoma and incomplete congenital glaucoma in two siblings. Acta Ophthalmol. 1984; 62: 359–63
- Shields M B, Buckley E, Klintworth G K, et al. Axenfeld–Rieger syndrome. A spectrum of developmental disorders. Surv Ophthalmol. 1985; 29: 387–409