1. A rare ANOS1 variant in siblings with Kallmann syndrome identified by whole exome sequencing. (6th December 2017) Authors: Lopategui, D. M.; Griswold, A. J.; Arora, H.; Clavijo, R. I.; Tekin, M.; Ramasamy, R. Journal: Andrology Issue: Volume 6:Number 1(2018) Page Start: 53 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗