Scavone, Maria, et al. “A Case of Kallmann Syndrome Associated to a Novel Missense Mutation of the FGFR1 Gene”.
Acta Biomedica Atenei Parmensis
, vol. 90, no. 4, Dec. 2019, pp. 577-9,
https://doi.org/10.23750/abm.v90i4.7170
.