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- 2020
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Mark
DIFFUSE RETINAL VASCULAR LEAKAGE AND CONE-ROD DYSTROPHY IN A FAMILY WITH THE HOMOZYGOUS MISSENSE C.1429G>A (P.GLY477ARG) MUTATION IN CRB1
(
- Contribution to journal › Article
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Mark
Severe retinitis pigmentosa phenotype associated with novel CNGB1 variants
(
- Contribution to journal › Article
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Mark
Analysis of retinal structure and function in cone dystrophy with supernormal rod response
2020) In Documenta Ophthalmologica(
- Contribution to journal › Article
- 2019
-
Mark
Non-syndromic retinal dystrophy associated with homozygous mutations in the ALMS1 gene
(
- Contribution to journal › Letter
- 2018
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Mark
Severe retinal degeneration at an early age in Usher syndrome type 1B associated with homozygous splice site mutations in MYO7A gene
(
- Contribution to journal › Article
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Mark
Novel causative variants in patients with achromatopsia
(
- Contribution to journal › Article
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Mark
Congenital stationary night blindness associated with morning glory disc malformation : a novel hemizygous mutation in CACNA1F
(
- Contribution to journal › Letter
- 2017
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Mark
Serous retinal detachment after panretinal photocoagulation for proliferative diabetic retinopathy : A case report
(
- Contribution to journal › Article