1. Loss of the imprinted, non-coding Snord116 gene cluster in the interval deleted in the Prader Willi syndrome results in murine neuronal and endocrine pancreatic developmental phenotypes. (6th September 2017) Authors: Burnett, Lisa Cole; Hubner, Gabriela; LeDuc, Charles A; Morabito, Michael V; Carli, Jayne F Martin; Leibel, Rudolph L Journal: Human molecular genetics Issue: Volume 26:Number 23(2017:Dec. 01) Page Start: 4606 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗