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You searched for: Author/Creator Capasso, Jenina

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1. A novel de novo intronic variant in ITPR1 causes Gillespie syndrome. Issue 8 (5th May 2021)

2. CNGB1‐related rod‐cone dystrophy: A mutation review and update. Issue 6 (16th May 2021)

3. Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders. Issue 17 (27th May 2021)

5. Macular cystoid spaces in patients with retinal dystrophy. (1st October 2016)