Philippe Bouchard

2 ta ish

Sorbonne University

1. Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2

   Catherine Dodé, Luís Teixeira, Jacqueline Levilliers +15

   Maqola20062 iqtibos

   ABIABI:AkademIndex/2026.other.720829

2. 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