Items where Division is "Institut für Humangenetik" and Year is 2021
![[up]](/style/images/multi_up.png)
Up a levelJump to: K
Number of items: 1.
K
Kollmeyer, Marie Luise (2021) The gastrointestinal phenotype of a mouse model for the neurodevelopmental disorder FOXP1 syndrome. [Abstract of a medical dissertation]
