Figure 5From: A rare de novo duplication of chromosome 21q22.12 → q22.3 with other concomitant deletion and duplication of small fragments in 21q associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization (A) Facial profile, hypertelorism, a depressed nasal bridge, a protruding tongue and (B) a single crease on the right hand at birth. Back to article page