Jean‐Claude Carel

2 ta ish

Hôpital Saint-Vincent-de-Paul

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

2. Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54

   Nicolás de Roux, Emmanuelle Génin, Jean‐Claude Carel +3

   Maqola20032 iqtibos

   ABIABI:AkademIndex/2026.other.720847