1. Endocrine phenotype of 6q16.1–q21 deletion involving SIM1 and Prader–Willi syndrome‐like features. Issue 12 (16th August 2013) Authors: Izumi, Kosuke; Housam, Ryan; Kapadia, Chirag; Stallings, Virginia A.; Medne, Livija; Shaikh, Tamim H.; Kublaoui, Bassil M.; Zackai, Elaine H.; Grimberg, Adda Journal: American journal of medical genetics Issue: Volume 161:Issue 12(2013:Dec.) Page Start: 3137 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Endocrine phenotype of 6q16.1–q21 deletion involving SIM1 and Prader–Willi syndrome‐like features. Issue 12 (16th August 2013) Authors: Izumi, Kosuke; Housam, Ryan; Kapadia, Chirag; Stallings, Virginia A.; Medne, Livija; Shaikh, Tamim H.; Kublaoui, Bassil M.; Zackai, Elaine H.; Grimberg, Adda Journal: American journal of medical genetics Issue: Volume 161:Issue 12(2013:Dec.) Page Start: 3137 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗