Chromosome 16p12.2-p11.2 deletion syndrome

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, Del(16)(p11.2p12.2), chromosome 16p12.2-p11.2 deletion syndrome, isolated cases, monosomy 16p11.2-p12.2, monosomy 16p11.2p12.2, chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-MB

1 clinical trial for this condition and its sub-types, 1 tagged with Chromosome 16p12.2-p11.2 deletion syndrome itself.