1. Co-occurrence of 16p13.11 microdeletion and ring chromosome 20 syndrome. (February 2016) Authors: Rodan, Lance H.; Zak, Maria; Stavropoulos, James; Joseph-George, Ann M.; Minassian, Berge A. Journal: Neurology Issue: Volume 2:Number 1(2016) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Severe rhizomelic shortening in a child with a complex duplication/deletion rearrangement of chromosome X. Issue 2 (22nd December 2017) Authors: Deshwar, Ashish R.; Dupuis, Lucie; Bergmann, Carsten; Stavropoulos, James; Mendoza‐Londono, Roberto Journal: American journal of medical genetics Issue: Volume 176:Issue 2(2018) Page Start: 450 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗