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Paper Details

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.
Ital J Pediatr
5
2018
Author NameAffiliation
Marzia PollazzonClinical Genetics Unit, AUSL-IRCCS of Reggio Emilia
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Release 1.2