Facetten
Zugriff
Einrichtung
Medientyp
Karte
Erscheinungsjahr
Autor/in
- Thiele, Holger
- Altmüller, Janine 6
- Schwedhelm, Edzard 5
- Büttner, Petra 4
- Bahls, Martin 3
- alle zeigen
Sprache
30 Einträge gefunden
-
-
-
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
-
De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients
- Hübers, Annemarie
- Just, Walter
- Rosenbohm, Angela
- Müller, Kathrin
- Marroquin, Nicolai
- Goebel, Ingrid
- Högel, Josef
-
Lack of association of a functional catechol-O-methyltransferase gene polymorphism with risk of tobacco smoking: results from a multicenter case-control study
- Mutschler, Jochen
- Abbruzzese, Elvira
- von der Goltz, Christoph
- Dinter, Christina
- Mobascher, Arian
- Thiele, Holger
- Diaz-Lacava, Amalia
-
Functional polymorphism in the neuropeptide Y gene promoter (rs16147) is associated with serum leptin levels and waist-hip ratio in women
- Mutschler, Jochen
- Abbruzzese, Elvira
- Wiedemann, Klaus
- von der Goltz, Christoph
- Dinter, Christina
- Mobascher, Arian
- Thiele, Holger
-
-
-
-