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ArticleItalian journal of pediatrics2018

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 anomalies.

I Maini et al.PubMed ↗Full text ↗Publisher ↗

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