1 – 3 of 3
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2020
-
Mark
Analysis of retinal structure and function in cone dystrophy with supernormal rod response
2020) In Documenta Ophthalmologica(
- Contribution to journal › Article
- 2018
-
Mark
Novel causative variants in patients with achromatopsia
(
- Contribution to journal › Article
-
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