-
1
-
-
0000265320
-
Anomalies in the size of the eye
-
Duke-Elder S, ed. St. Louis, MO: Mosby-Year Book
-
Duke-Elder S. Anomalies in the size of the eye. In: Duke-Elder S, ed. System of Ophthalmology. St. Louis, MO: Mosby-Year Book; 1963; 488-495.
-
(1963)
System of Ophthalmology
, pp. 488-495
-
-
Duke-Elder, S.1
-
2
-
-
0027293603
-
Classification of microphthalmos and coloboma
-
Warburg M. Classification of microphthalmos and coloboma. J Med Genet. 1993;30:664-669.
-
(1993)
J Med Genet
, vol.30
, pp. 664-669
-
-
Warburg, M.1
-
4
-
-
4744346127
-
Evaluation of normal corneas using the scanning-slit topography/ pachymetry system
-
Módis L, Langenbucher A, Seitz B. Evaluation of normal corneas using the scanning-slit topography/pachymetry system. Cornea. 2004;23:689-694.
-
(2004)
Cornea
, vol.23
, pp. 689-694
-
-
Módis, L.1
Langenbucher, A.2
Seitz, B.3
-
5
-
-
0001695559
-
Ray tracing through non-spherical surfaces
-
Baker TY. Ray tracing through non-spherical surfaces. Proc Phys Soc. 1943;55:361-364.
-
(1943)
Proc Phys Soc
, vol.55
, pp. 361-364
-
-
Baker, T.Y.1
-
6
-
-
0027462648
-
Mathematical models of the general corneal surface
-
Burek H, Douthwaite WA. Mathematical models of the general corneal surface. Ophthal Physiol Opt. 1993;13:68-72.
-
(1993)
Ophthal Physiol Opt
, vol.13
, pp. 68-72
-
-
Burek, H.1
Douthwaite, W.A.2
-
7
-
-
0022000854
-
Bilateral nanophthalmos, pigmentary retinal dystrophy and angle closure glaucoma - A new syndrome?
-
Ghose S, Sachdev MS, Kumar H. Bilateral nanophthalmos, pigmentary retinal dystrophy and angle closure glaucoma - a new syndrome? Br J Ophthalmol. 1985;69:624-628.
-
(1985)
Br J Ophthalmol
, vol.69
, pp. 624-628
-
-
Ghose, S.1
Sachdev, M.S.2
Kumar, H.3
-
9
-
-
0033504352
-
Retinitis pigmentosa, nanophthalmos and optic disc drusen. A case report
-
Buys YM, Pavlin CJ. Retinitis pigmentosa, nanophthalmos and optic disc drusen. A case report. Ophthalmology. 1999;106:619-622.
-
(1999)
Ophthalmology
, vol.106
, pp. 619-622
-
-
Buys, Y.M.1
Pavlin, C.J.2
-
10
-
-
0032797310
-
Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32
-
Bessant DAR, Anwar K, Khaliq S, et al. Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32. Br J Ophthalmol. 1999;83:919-922.
-
(1999)
Br J Ophthalmol
, vol.83
, pp. 919-922
-
-
Bessant, D.A.R.1
Anwar, K.2
Khaliq, S.3
-
12
-
-
0032767869
-
Evaluation of corneal thickness and topography in normal eyes using the Orbscan corneal topography system
-
Liu Z, Huang AJ, Pflugfelder SC. Evaluation of corneal thickness and topography in normal eyes using the Orbscan corneal topography system. Br J Ophthalmol. 1999;83:774-778.
-
(1999)
Br J Ophthalmol
, vol.83
, pp. 774-778
-
-
Liu, Z.1
Huang, A.J.2
Pflugfelder, S.C.3
-
13
-
-
0025322759
-
Classification of normal corneal topography based on computer-assisted videokeratography
-
Bogan SJ, Waring GO III, Ibrahim O, et al. Classification of normal corneal topography based on computer-assisted videokeratography. Arch Ophthalmol. 1990;108:945-949.
-
(1990)
Arch Ophthalmol
, vol.108
, pp. 945-949
-
-
Bogan, S.J.1
Waring III, G.O.2
Ibrahim, O.3
-
15
-
-
0032231633
-
Autosomal dominant Nanophthalmos (NNO1) with high hyperopia and angle closure glaucoma maps to chromosome 11
-
Othman MI, Sullivan SA, Skuta GL, et al. Autosomal dominant Nanophthalmos (NNO1) with high hyperopia and angle closure glaucoma maps to chromosome 11. Am J Hum Genet. 1998;63:1411-1418.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1411-1418
-
-
Othman, M.I.1
Sullivan, S.A.2
Skuta, G.L.3
-
16
-
-
4043103363
-
Physical and transcript map of the autosomal dominant colobomatous microphthalmia locus on chromosome15q12-q15 and refinement to a 4.4Mb region
-
Michon L, Morle L, Bozon M, et al. Physical and transcript map of the autosomal dominant colobomatous microphthalmia locus on chromosome15q12-q15 and refinement to a 4.4Mb region. Eur J Hum Genet. 2004;12:574-578.
-
(2004)
Eur J Hum Genet
, vol.12
, pp. 574-578
-
-
Michon, L.1
Morle, L.2
Bozon, M.3
-
17
-
-
0031971589
-
A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32
-
Bessant DAR, Khaliq S, Hameed A, et al. A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32. Am J Hum Genet. 1998;62:1113-1116.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1113-1116
-
-
Bessant, D.A.R.1
Khaliq, S.2
Hameed, A.3
-
18
-
-
0034425404
-
Human microphthalmia associated with mutations in the retinal homeobox gene CHX10
-
Percin EF, Ploder LA, Yu JJ, et al. Human microphthalmia associated with mutations in the retinal homeobox gene CHX10. Nat Genet. 2000;25:397-401.
-
(2000)
Nat Genet
, vol.25
, pp. 397-401
-
-
Percin, E.F.1
Ploder, L.A.2
Yu, J.J.3
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