Figure 1From: De novoframeshift mutation in ASXL3 in a patient with global developmental delay, microcephaly, and craniofacial anomalies Patient at 6 years of age. Note microcephaly, trigoncephaly, hypertelorism, upslanting palpebral fissures, epicanthal folds, periorbital fullness, anteverted nares, and posteriorly rotated ears.Back to article page