Fig. 1
From: Novel pathogenic variants and multiple molecular diagnoses in neurodevelopmental disorders
a-f Composite figures of genes with pathogenic or likely pathogenic variants identified in this study: CDK13, CHD4, KCNQ3, KMT5B, TCF20, and ZBTB18 (adapted from the “Prevalence and architecture of de novo mutations in developmental disorders” study [9]). Boxes: pink highlighted variants are VUS and red highlighted variants are pathogenic or likely pathogenic changes. Functional domains of the encoded protein are indicated by blue boxes. Variants that have already been identifeid in the previous study are shown with red branching