ArticleGenes2023
A Novel 13q12 Microdeletion Associated with Familial Syndromic Corneal Opacification.
Jasmine Y Serpen et al.PubMed ↗Full text ↗Publisher ↗
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ArticleGenes2023
Jasmine Y Serpen et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.