SETBP1 and cranioectodermal dysplasia: Some examples of new disease-associated genes that have been discovered using NGS technologies are DHODH [8], the causative gene of the Miller syndrome, WDR35, the gene that is responsible for Sensenbrenner syndrome [9], and SETBP1, which is responsible for the Schinzel–Giedion syndrome (SGS) [10].