20p12.3 microdeletion syndrome
From BugSigDB
20p12.3 microdeletion syndrome is a recently described syndrome characterized by Wolff-Parkinson-White syndrome (see this term), variable developmental delay and facial dysmorphism.
- Aliases
- 20p12.3 microdeletion syndrome
- Del(20)(p12.3)
- Monosomy 20p12.3
- monosomy 20p12.3
