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- 2003
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Mark
Mutation screening of patients with Leber congenital amaurosis or the enhanced S-cone syndrome reveals a lack of sequence variations in the NRL gene
(
- Contribution to journal › Article
- 1998
-
Mark
Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype
(
- Contribution to journal › Article
-
Mark
Phenotype in a Swedish family with X-linked retinitis pigmentosa caused by a novel splice defect in the RPGR gene
(
- Contribution to journal › Article
- 1997
-
Mark
Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene
(
- Contribution to journal › Article