Original Article Published: 30 September 2010 Identification of a microdeletion at Xp22.13 in a Taiwanese family presenting with Nance-Horan syndrome Hsiao-Mei Liao, Dau-Ming Niu, Yan-Jang Chen ...

A microdeletion was identified on chromosome 21 involving a 3.1-Mb segment from 21q22.11 to 21q22.12, indicating partial monosomy for this region.

Study: PARK2 Microdeletion or Duplications Have Been Implicated in Different Neurological Disorders Including Early Onset Parkinson Diseas e. Image Credit: MattLphotography / Shutterstock About ...

Blanchard was first diagnosed with microdeletion 1Q21.1 in 2012 Gypsy-Rose Blanchard's daughter has not inherited the rare genetic condition that she has. On Wednesday, April 23, the 33-year-old ...