Associated Papers
Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs*6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing.
Zhuang J et al.
Frontiers in Genetics, 2022
Novel BCOR mutations in patients with oculofaciocardiodental (OFCD) syndrome.
Feberwee HE et al.
Clinical Genetics, 2014
Oculofaciocardiodental syndrome: a rare case and review of the literature.
Davoody A et al.
The Cleft Palate-craniofacial Journal : Official Publication of the American Cleft Palate-craniofacial Association, 2012
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