Chromosome 16p12.2-p11.2 deletion syndrome
Chromosome 16p12.2-p11.2 deletion syndrome
Definition
16p11.2-p12.2 microdeletion syndrome is a recently described syndrome characterized by developmental delay and facial dysmorphism.
Also known as 16p11.2-p12.2 microdeletion syndrome, 16p11.2p12.2 microdeletion syndrome, chromosome 16p12.2-p11.2 deletion syndrome, isolated cases, Del(16)(p11.2p12.2), monosomy 16p11.2-p12.2, monosomy 16p11.2p12.2 — per MONDO