Rafael Filippelli-Silva
0000-0002-5723-8330
UNIFESP
3 papers found
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Analysis of an NGS retinopathy panel detects chromosome 1 uniparental isodisomy in a patient with RPE65-related leber congenital amaurosis
Relative frequency of inherited retinal dystrophies in Brazil
The correlation between CRB1 variants and the clinical severity of Brazilian patients with different inherited retinal dystrophy phenotypes
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