Fig. 1From: Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical features of 293 children with neurodevelopmental disorders and/or multiple congenital anomaliesDescription of the total sample enrolled investigated through aCGH until 07–31-2016. Red rectangle includes the patient group (293/339) on which the statistical analysis was performedBack to article page