Hochschulschrift
Cross-sectional phenotypical differentiation of major blinding eye diseases in Europe: inherited retinal dystrophies in focus
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISBN
-
9783844002065
- Dimensions
-
21 cm, 227 g
- Extent
-
V, 112, [30] S.
- Language
-
Englisch
- Notes
-
graph. Darst.
Zugl.: Tübingen, Univ., Diss., 2011
- Keyword
-
Netzhautdegeneration
Erbkrankheit
Epidemiologie
Differentialdiagnose
Netzhautkrankheit ; Epidemiologie ; Europa
- Event
-
Veröffentlichung
- (where)
-
Aachen
- (who)
-
Shaker
- (when)
-
2011
- Creator
-
Prokofyeva, Elena
- Table of contents
- Rights
-
Bei diesem Objekt liegt nur das Inhaltsverzeichnis digital vor. Der Zugriff darauf ist unbeschränkt möglich.
- Last update
-
11.06.2025, 1:41 PM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Object type
- Hochschulschrift
Associated
- Prokofyeva, Elena
- Shaker
Time of origin
- 2011
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Deletions and Functional Assessment of Exonic Variants affecting Splicing in Genes underlying Inherited Retinal Dystrophies
Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies
Cross-sectional phenotypical differentiation of major blinding eye diseases in Europe : inherited retinal dystrophies in focus
Relative frequency of inherited retinal dystrophies in Brazil
Early Visual Symptom Patterns in Inherited Retinal Dystrophies
The genetic landscape of inherited retinal dystrophies in Arabs
Retina regeneration : new strategies to treat inherited retinal dystrophies
Quantitative genomics : influence of gene expression on inherited retinal dystrophies
Reviewing the Role of Ultra-Widefield Imaging in Inherited Retinal Dystrophies
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A pilot investigation of audiovisual processing and multisensory integration in patients with inherited retinal dystrophies
Deletions and Functional Assessment of Exonic Variants affecting Splicing in Genes underlying Inherited Retinal Dystrophies