Rafael Filippelli-Silva

3PUBLICATIONS
3CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Gene mapping
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Publications (3)

|Jun 23, 2021
Analysis of an NGS retinopathy panel detects chromosome 1 uniparental isodisomy in a patient with RPE65-related leber congenital amaurosis.

Fabiana Louise Motta, Rafael Filippelli-Silva, Joao Paulo Kitajima

|Oct 31, 2018
Relative frequency of inherited retinal dystrophies in Brazil.

Fabiana Louise Motta, Renan Paulo Martin, Rafael Filippelli-Silva

|Aug 19, 2017
The correlation between CRB1 variants and the clinical severity of Brazilian patients with different inherited retinal dystrophy phenotypes.

Fabiana Louise Motta, Mariana Vallim Salles, Karita Antunes Costa

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Frequent Collaborators

1 joint publications

Mariana Vallim Salles

1 joint publications

Fabiana Louise Motta

1 joint publications

Juliana Maria Ferraz Sallum