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- 1999
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Mark
Digenic inheritance of a ROM1 gene mutation with a peripherin/RDS or rhodopsin mutation in families with retinitis pigmentosa
(
- Contribution to journal › Article
- 1998
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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
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Mark
Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype
(
- 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
-
Mark
A Swedish family with a mutation in the peripherin/RDS gene (Arg-172-Trp) associated with a progressive retinal degeneration
(
- Contribution to journal › Article
- 1997
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Mark
A mild phenotype of autosomal dominant retinitis pigmentosa is associated with the rhodopsin mutation Pro-267–Leu
(
- Contribution to journal › Article
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Mark
Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene
(
- Contribution to journal › Article
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Mark
Autosomal dominant retinitis pigmentosa with a rhodopsin mutation (Arg-135–Trp): Disease phenotype in a Swedish family
(
- Contribution to journal › Article
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Mark
Phenotypes and genotypes in families with hereditary tapetoretinal degenerations
1997)(
- Thesis › Doctoral thesis (compilation)
- 1995
-
Mark
Phenotype variation within a choroideremia family lacking the entire CHM gene
(
- Contribution to journal › Article