1. Deletion of UBE3A in brothers with Angelman syndrome at the breakpoint with an inversion at 15q11.2. Issue 11 (6th August 2014) Authors: Kuroda, Yukiko; Ohashi, Ikuko; Saito, Toshiyuki; Nagai, Jun‐Ichi; Ida, Kazumi; Naruto, Takuya; Wada, Takahito; Kurosawa, Kenji Journal: American journal of medical genetics Issue: Volume 164:Issue 11(2014.) Page Start: 2873 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Microdeletion of 19p13.3 in a girl with Peutz–Jeghers syndrome, intellectual disability, hypotonia, and distinctive features. (8th December 2014) Authors: Kuroda, Yukiko; Saito, Toshiyuki; Nagai, Jun‐Ichi; Ida, Kazumi; Naruto, Takuya; Masuno, Mitsuo; Kurosawa, Kenji Journal: American journal of medical genetics Issue: Volume 167:Number 2(2015:Feb.) Page Start: 389 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗