1 – 2 of 2
- show: 15
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2012
-
Mark
Mutations in RPGR and RP2 Account for 15% of Males with Simplex Retinal Degenerative Disease
(
- Contribution to journal › Article
- 2003
-
Mark
Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes
(
- Contribution to journal › Article