Facetten
Zugriff
Einrichtung
Medientyp
- Text 7
Karte
Erscheinungsjahr
Autor/in
- Gal, Andreas
- Kurth, Ingo 2
- Orth, Ulrike 2
- Alessandro, Silvio 1
- Altmann, Jens 1
- alle zeigen
Sprache
- Deutsch 7
7 Einträge gefunden
-
-
Ultra high throughput sequencing excludes MDH1 as candidate gene for RP28-linked retinitis pigmentosa.
- Frio, Thomas Rio
- Panek, Sylwia
- Iseli, Christian
- Gioia, Di
- Alessandro, Silvio
- Gal, Andreas
- Gal, Andreas
-
A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa.
- Azam, Maleeha
- Khan, Muhammad Imran
- Gal, Andreas
- Hussain, Alamdar
- Shah, Syed Tahir Abbas
- Khan, Muhammad Shakil
- Sadeque, Ahmed
-
RDH12 Activity and Effects on Retinoid Processing in the Murine Retina.
- Chrispell, Jared D
- Feathers, Kecia L
- Kane, Maureen A
- Kim, Chul Y
- Brooks, Matthew
- Khanna, Ritu
- Kurth, Ingo
-
-
Duplications of noncoding elements 5' of SOX9 are associated with brachydactyly-anonychia.
- Kurth, Ingo
- Klopocki, Eva
- Stricker, Sigmar
- van Oosterwijk, Jolieke
- Vanek, Sebastian
- Altmann, Jens
- Santos, Heliosa G
-