Facetten
Zugriff
Einrichtung
Medientyp
- Text 3
Karte
Erscheinungsjahr
Autor/in
- Thoenes, Michaela
- Nürnberg, Gudrun 2
- Ahmad, Adeel 1
- Ahmad, Jamil 1
- Altmüller, Janine 1
- alle zeigen
Sprache
- Englisch 3
3 Einträge gefunden
-
A TUBB6 mutation is associated with autosomal dominant non-progressive congenital facial palsy, bilateral ptosis and velopharyngeal dysfunction
- Fazeli, Walid
- Herkenrath, Peter
- Stiller, Barbara
- Neugebauer, Antje
- Fricke, Julia
- Lang-Roth, Ruth
- Nürnberg, Gudrun
-
OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67)
- Thoenes, Michaela
- Zimmermann, Ulrike
- Ebermann, Inga
- Ptok, Martin
- Lewis, Morag A
- Thiele, Holger
- Morlot, Susanne
-
Identification of a novel LCA5 mutation in a Pakistani family with Leber congenital amaurosis and cataracts.
- Ahmad, Adeel
- Daud, Shakeela
- Kakar, Naseebullah
- Nürnberg, Gudrun
- Nürnberg, Peter
- Babar, Masroor Ellahi
- Thoenes, Michaela