Mutations in the NKX2.1 and the PAX8 genes in a boy with thyroid dysgenesis, respiratory and neurological disorders

Abstract

s of the 51st Workshop for Pediatric Research 51st Workshop for Pediatric Research Göttingen, Germany

Cite this paper

@inproceedings{Hermanns2015MutationsIT, title={Mutations in the NKX2.1 and the PAX8 genes in a boy with thyroid dysgenesis, respiratory and neurological disorders}, author={Pia Hermanns and Małgorzata Kumorowicz-Czoch and Joachim Pohlenz}, year={2015} }