Stefan Vermeulen

1 ta ish

Ghent University Hospital

1. Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

   Catherine Dodé, Jacqueline Levilliers, Jean‐Michel Dupont +27

   Maqola20032 iqtibos

   ABIABI:AkademIndex/2026.other.720840