Related Experiment Video
Updated: Feb 11, 2026

08:42
Skeletal Phenotype Analysis of a Conditional Stat3 Deletion Mouse Model
Published on: July 3, 2020
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DiGeorge phenotype in the absence of 22q11 deletion - a case report
Images in Paediatric Cardiology
|May 8, 2018
Abstract:
DiGeorge syndrome is polytopic developmental field defect which is usually associated with 22q11.2 microdeletion. However, this phenotype may be caused by other conditions. We report such a case and briefly review these alternative causes for this particular phenotype.
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