Category:Sclerocornea

Media in category "Sclerocornea"

The following 9 files are in this category, out of 9 total.

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  Distinct Roles of Histone Lysine Demethylases and Methyltransferases in Developmental Eye Disease.jpg 936 × 761; 844 KB
  
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  Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma.jpg 555 × 409; 103 KB
  
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  Human eyeball with phenotypic expression of aniridia with PAX6 gene mutation.jpg 1,200 × 857; 129 KB
  
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  Iraqi Girl Travels to U.S. in Effort to Repair Vision.jpg 1,024 × 678; 335 KB
  
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  Ocular images from individuals with ARHGAP35 variants.jpg 1,520 × 1,354; 1.41 MB
  
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  Phenotypic appearance in patients with sclerocornea, aphakia, and microphthalmia.jpg 544 × 402; 235 KB
  
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  Photographs of the six patients with MLS syndrome and a heterozygous HCCS mutation or Xp22 monosomy.jpg 1,200 × 664; 619 KB
  
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  Portrait images of patients with a mutation in the SOX2 gene.jpg 1,101 × 682; 619 KB
  
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  Sclerocornea, i.e., peripheral scleralization of the cornea, accompanied by the feature of cornea plana (CNA2, OMIM 217300).jpg 819 × 572; 347 KB