Jean‐Pierre Hardelin

2 ta ish

Pasteur Institute

1. The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

   Renaud Legouis, Jean‐Pierre Hardelin, Jacqueline Levilliers +7

   Maqola19912 iqtibos

   ABIABI:AkademIndex/2026.other.720837

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