16p11.2p12.2 microdeletion syndrome
From BugSigDB
16p11.2-p12.2 microdeletion syndrome is a recently described syndrome characterized by developmental delay and facial dysmorphism.
- Aliases
- 16p11.2-p12.2 microdeletion syndrome
- Del(16)(p11.2p12.2)
- Monosomy 16p11.2-p12.2
- Monosomy 16p11.2p12.2
