A higher rare CNV burden in the genetic background potentially contributes to intellectual disability phenotypes in 22q11.2 deletion syndrome.
| Image |  |
|---|---|
| Description | scientific article published on 27 November 2017 |
| Author/s |
author: Frank Kooy Santhosh Girirajan |
| Publication date | November 28, 2017 |
| Language | |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |