19p13.12 microdeletion syndrome
From BugSigDB
19p13.12 microdeletion syndrome is a newly described syndrome characterized by moderate to severe developmental delay, language delay, bilateral sensorineural and/or conductive hearing loss and facial dysmorphism.
- Aliases
- 19p13.12 microdeletion syndrome
- Chromosome19p13.12 microdeletion
- Del(19)(p13.12)
- Monosomy 19p13.12
- monosomy 19p13.12
