Publication
Title
A higher rare CNV burden in the genetic background potentially contributes to intellectual disability phenotypes in 22q11.2 deletion syndrome
Author
Abstract
Language
English
Source (journal)
European journal of medical genetics. - Paris
Publication
Paris : 2018
ISSN
1769-7212
Volume/pages
61:4(2018), p. 209-212
ISI
000427490300006
Full text (Publisher's DOI)
UAntwerpen
Faculty/Department
Research group
Publication type
Subject
Affiliation
Publications with a UAntwerp address
External links
Web of Science
Record
Identification
Creation 04.05.2018
Last edited 10.12.2018
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