Fig. 2: Novel RARB genetic variants in the patients.
From: Clinical features of syndromic microphthalmia in two novel RARB variants

A Case 1 had a rare heterozygous frameshift variant in RARB, c.1205_1206del. No heterozygous variant was identified in the father or mother. B Case 2 had a rare heterozygous missense in RARB, c.844G>T. No heterozygous variant was identified in the father or mother.