Dissertationen der Medizinischen Fakultät
Browse by Advisor: Rappold, Prof. Dr. rer. nat. Gudrun
2022
Rheinert, David (2022) Vom Gen zum Phänotyp : die SHOX-Gene und ihr Netzwerk.
2021
Kollmeyer, Marie Luise (2021) The gastrointestinal phenotype of a mouse model for the neurodevelopmental disorder FOXP1 syndrome.
2019
Linz, Valerie Catherine (2019) Investigating the gastrointestinal phenotype in a knockout mouse model with a specific loss of Foxp1 (forkhead box protein P1) in neurons.
Simm, Franziska (2019) Expanding the molecular spectrum of combined pituitary hormone deficiency.
2018
Vogel, Ralf (2018) Untersuchung der 17β-Hydroxysteroid-Dehydrogenase Typ 10 und deren Mutanten auf Funktionen des Poly(C)-Bindeproteins 1.
2017
Rafiullah, Rafiullah (2017) Identification and characterization of genes underlying intellectual disability and autism spectrum disorders.