In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?

In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?

Abstract Background 22q11.2 deletion syndrome (22q11DS), a copy number variation (CNV) disorder, occurs in approximately 1:4000 live births due to a heterozygous microdeletion at position 11.2 (proximal) on the q arm of human chromosome 22 (hChr22) (McDonald-McGinn and Sullivan, Medicine 90:1-18, 20...

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Bibliographic Details
Main Authors: Zahra Motahari, Sally Ann Moody, Thomas Michael Maynard, Anthony-Samuel LaMantia
Format: Article
Language:English
Published: BMC 2019-06-01
Series:Journal of Neurodevelopmental Disorders
Subjects:
22q11DS
Neural development
Cognition
Cardiovascular
Craniofacial
Copy number variants
Online Access:http://link.springer.com/article/10.1186/s11689-019-9267-z

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http://link.springer.com/article/10.1186/s11689-019-9267-z

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