REFERENCES
- Huret J L, Leonard C, Forestier G, Rethore M O, Lejeune J. Eleven New cases of del (9p) and features from 80 cases. J Med Genet. 1988; 25: 741–749
- Broughton W L, Rosebaum K N, Beauchamp G R. Congenital glaucoma and other ocular abnormalities associated with pericentric inversion of Chromosone 11. Arch Ophthalmol. 1983; 101: 594–597
- Smith D W. Recognizable patterns of human malformation (genetic embryologic and clinical aspects), 4th ed. WB Saunders, Philadelphia 1988; 44–45
- Katsushima H, Kii T, Soma K, Ohyanagi K, Niikawa N. Primary congenital glaucoma in a patient with trisomy 2q (q33-qter) and monosomy 9p (p24-pter). Arch Ophthalmol. 1987; 105: 323–324
- Verbraak F D, Pogany K, Pillon J W, Mooy C M, De France H F, Hennekam R CM, Bleeker-Wagemakers E M. Congenital glaucoma in a child with partial 1q duplication and 9p deletion. Ophthalm Paed Genet. 1992; 13: 165–170
- Wahram J, Atidia J, Goitein R, Cohen T. Pericentre inversions of chromosone 9 in two families. Cytogenet Cell Genet. 1972; 11: 132–144
- Cohn A C, Kearns L S, Savarirayan R, Ryan J, Craig J E, Mackey D A. Chromosomal abnormalities and glaucoma: A case of congenital glaucoma with trisomy 8q22-Qter/Monosomy 9p23-Pter. Ophthalmic Genet. 2005; 26(1)45–53