Characterization of a complex rearrangement involving duplication and deletion of 9p in an infant with craniofacial dysmorphism and cardiac anomalies

DOI: 10.1186/1755-8166-5-31

Keywords: Concomitant deletion and duplication of 9p, Deletion 9p Syndrome, Duplication 9p Syndrome, Craniofacial dysmorphism, Cardiac anomalies

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