(1)
Scavone, M. .; Chiarello, P. .; Talarico, V. .; Mascaro, I. .; Caglioti, C. .; Galati, M. C. .; Raiola, G. A Case of Kallmann Syndrome Associated to a Novel Missense Mutation of the FGFR1 Gene. Acta Biomed 2019, 90, 577-579.