Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs*6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing

Overview of attention for article published in Frontiers in Genetics, March 2022

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New Research: Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs*6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing: Background: Oculofaciocardiodental (OFCD) syndrome is an X-linked… https://t.co/AxvVz

26 Mar 2022

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