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- 2016
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Mark
Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing.
(
- Contribution to journal › Article
- 2012
-
Mark
Mutations in RPGR and RP2 Account for 15% of Males with Simplex Retinal Degenerative Disease
(
- Contribution to journal › Article
-
Mark
Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database
(
- Contribution to journal › Article