Associated Papers
Genetic analysis of axial length genes in high grade myopia from Indian population.
Sharmila F et al.
Meta Gene, 2014
Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophy.
Iseri SU et al.
Human Genetics, 2010
Genetic analysis of SOX2 and VSX2 genes in 27 Egyptian families with anophthalmia and microphthalmia.
Ammar THA et al.
Ophthalmic Genetics, 0
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