Autor/in Alawi, Malik Borkhardt, Arndt Kortüm, Fanny Kutsche, Kerstin Mayatepek, Ertan 1 Schmidt-Jiménez, Leon F 1 Velleuer, Eunike 1 Vogel, Markus 1 alle zeigenListe einklappen
Homozygous HOXB1 loss-of-function mutation in a large family with hereditary congenital facial paresis Vogel, Markus Velleuer, Eunike Schmidt-Jiménez, Leon F Mayatepek, Ertan Borkhardt, Arndt Alawi, Malik Kutsche, Kerstin 2016 - Forschungsinformationssystem des UKE
