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Arch Ophthalmol. 1990;108(10):1407-1407. doi:10.1001/archopht.1990.01070120055028
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In the article by Aguirre Vila-Coro entitled "Vascular Microdissection in Strabismus Surgery," published in the July 1990 issue of the Archives (1990;108:1034-1036), Figs 1 and 2 were transposed and printed upside down. The legends, however, were printed in the correct positions.

REFERENCES

Nikoskelainen EK, Savontaus ML, Wanne OP, Katila MJ, Nummelin KU.  Leber's hereditary optic neuroretinopathy, a maternally inherited disease: a geneologic study in four pedigrees . Arch Ophthalmol . 1987;;105:665-671.
Wallace DC, Singh G, Lott MT, et al.  Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy . Science . 1988;;242:1427-1430.
Stone EM, Coppinger JM, Kardon RH, Donelson J.  Mae III positively detects the mitochondrial mutation associated with type I Leber's hereditary optic neuropathy . Arch Ophthalmol . 1990;;108:1417-1420.
Johns DR. Improved molecular genetic diagnosis of Leber's hereditary optic neuropathy. N Engl J Med. 1990. In press.
Vilkki J, Savontaus M-L, Nikoskelainen EK.  Genetic heterogeneity in Leber's hereditary optic neuropathy revealed by mitochondrial DNA polymorphism . Am J Hum Genet . 1989;;45:206-211.
Holt IJ, Miller DH, Harding AE.  Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy . J Med Genet . 1989;;26:739-743.
Lott MY, Voljavec AS, Wallace DC.  Variable genotype of Leber's hereditary optic neuropathy patients . Am J Ophthalmol . 1990;;109:625-631.
Chen J-D, Cox I, Denton MJ.  Preliminary exclusion of an X-linked gene in Leber optic atrophy by linkage analysis . Hum Genet . 1989;;82:203-207.

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Nikoskelainen EK, Savontaus ML, Wanne OP, Katila MJ, Nummelin KU.  Leber's hereditary optic neuroretinopathy, a maternally inherited disease: a geneologic study in four pedigrees . Arch Ophthalmol . 1987;;105:665-671.
Wallace DC, Singh G, Lott MT, et al.  Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy . Science . 1988;;242:1427-1430.
Stone EM, Coppinger JM, Kardon RH, Donelson J.  Mae III positively detects the mitochondrial mutation associated with type I Leber's hereditary optic neuropathy . Arch Ophthalmol . 1990;;108:1417-1420.
Johns DR. Improved molecular genetic diagnosis of Leber's hereditary optic neuropathy. N Engl J Med. 1990. In press.
Vilkki J, Savontaus M-L, Nikoskelainen EK.  Genetic heterogeneity in Leber's hereditary optic neuropathy revealed by mitochondrial DNA polymorphism . Am J Hum Genet . 1989;;45:206-211.
Holt IJ, Miller DH, Harding AE.  Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy . J Med Genet . 1989;;26:739-743.
Lott MY, Voljavec AS, Wallace DC.  Variable genotype of Leber's hereditary optic neuropathy patients . Am J Ophthalmol . 1990;;109:625-631.
Chen J-D, Cox I, Denton MJ.  Preliminary exclusion of an X-linked gene in Leber optic atrophy by linkage analysis . Hum Genet . 1989;;82:203-207.

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