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- 1998
-
Mark
Phenotypic expression of autosomal dominant retinitis pigmentosa in a Swedish family expressing a Phe-211-Leu variant of peripherin/RDS
(
- Contribution to journal › Article
-
Mark
Detection of alterations in all three exons of the peripherin/RDS gene in Swedish patients with retinitis pigmentosa using an efficient DGGE system
(
- Contribution to journal › Article
- 1997
-
Mark
Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: Paucity of mutations in the coding region, but splice defects in two families
(
- Contribution to journal › Article
-
Mark
A mild phenotype of autosomal dominant retinitis pigmentosa is associated with the rhodopsin mutation Pro-267–Leu
(
- Contribution to journal › Article
-
Mark
Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene
(
- Contribution to journal › Article
-
Mark
Autosomal dominant retinitis pigmentosa with a rhodopsin mutation (Arg-135–Trp): Disease phenotype in a Swedish family
(
- Contribution to journal › Article
- 1995
-
Mark
Phenotype variation within a choroideremia family lacking the entire CHM gene
(
- Contribution to journal › Article
- 1992
-
Mark
A six generation family with autosomal dominant retinitis pigmentosa and a rhodopsin gene mutation (arginine-135–leucine)
(
- Contribution to journal › Article
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