Fig. 1: Facial appearance of patients with JARID2 deletions and single-nucleotide variants.
From: JARID2 haploinsufficiency is associated with a clinically distinct neurodevelopmental syndrome
Individual 1 (a), individual 2 (b), individual 3 (c), individual 5 (d), individual 6 (who is the father of individual 5) (e), individual 7 (f), individual 11 (g), individual 14 (h), and individual 16 (i). Some individuals share physical features similar to others in the literature with JARID2-plus deletions, including high anterior hairline, broad forehead, deep set eyes, infraorbital dark circles, depressed nasal bridge, bulbous nasal tip and full lips.
