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Medientyp
- Text 2
Karte
Erscheinungsjahr
Autor/in
- Nürnberg, Gudrun
- Thoenes, Michaela
- Ahmad, Adeel 1
- Ahmad, Jamil 1
- Altmüller, Janine 1
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Sprache
- Englisch 2
2 Einträge gefunden
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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
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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