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- 2018
-
Mark
Severe retinal degeneration at an early age in Usher syndrome type 1B associated with homozygous splice site mutations in MYO7A gene
(
- Contribution to journal › Article
- 2016
-
Mark
Characterization of macular structure and function in two swedish families with genetically identified autosomal dominant retinitis pigmentosa
(
- Contribution to journal › Article
- 2007
-
Mark
Intracellular mechanisms in rd1 mouse retinal degeneration
2007) In Lund University Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
-
Mark
Calpain activity in retinal degeneration.
(
- Contribution to journal › Scientific review
- 2006
-
Mark
Evaluation of the visual pathway with ERG, mfERG and mfVEP in inherited eye disorders
2006)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Ames Waltzer deaf mice have reduced electroretinogram amplitudes and complex alternative splicing of Pcdh15 transcripts
(
- Contribution to journal › Article
- 1999
-
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
-
Mark
Gör balansprov på alla döva småbarn! : Tidig upptäckt av Ushers syndrom ökar möjligheterna till kommunikation vid senare dövblindhet
(
- Contribution to journal › Article
- 1997
-
Mark
Phenotypes and genotypes in families with hereditary tapetoretinal degenerations
1997)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Usher's syndrome and cochlear implant
(
- Contribution to journal › Debate/Note/Editorial