Sort   by:  
 Page size 
UnknownGenotype-Phenotype Correlations in Corneal Dystrophies: Advances in Molecular Genetics and Therapeutic Insights.
Not available
S-EPMC11962681 | biostudies-literature
UnknownReplication of SNP associations with keratoconus in a Czech cohort.
Not available
S-EPMC5313182 | biostudies-literature
UnknownActive transforming growth factor-β2 in the aqueous humor of posterior polymorphous corneal dystrophy patients.
Not available
S-EPMC5393593 | biostudies-literature
UnknownValidation of rs2956540:G>C and rs3735520:G>A association with keratoconus in a population of European descent.
Not available
S-EPMC4613460 | biostudies-literature
UnknownMacular corneal dystrophy and associated corneal thinning.
Not available
S-EPMC4194335 | biostudies-literature
UnknownClinical and Genetic Study of X-Linked Juvenile Retinoschisis in the Czech Population.
Not available
S-EPMC8623540 | biostudies-literature
UnknownSchnyder corneal dystrophy and associated phenotypes caused by novel and recurrent mutations in the UBIAD1 gene.
Not available
S-EPMC6142341 | biostudies-literature
UnknownSnail Track Lesion with Flat Keratometry in Anterior Segment Dysgenesis Caused by a Novel FOXC1 Variant.
Not available
S-EPMC9457150 | biostudies-literature
UnknownPseudodominant Nanophthalmos in a Roma Family Caused by a Novel PRSS56 Variant.
Not available
S-EPMC7212339 | biostudies-literature
UnknownNon-Penetrance for Ocular Phenotype in Two Individuals Carrying Heterozygous Loss-of-Function <i>ZEB1</i> Alleles.
Not available
S-EPMC8146820 | biostudies-literature
Sort   by:  
 Page size