• A case of oculo-facio-cardio-dental syndrome with integrated orthodontic-prosthodontic treatment
• A family of oculofaciocardiodental syndrome (OFCD) with a novel BCOR mutation and genomic rearrangements involving NHS
• A novel deletion mutation in the BCOR gene is associated with oculo-facio-cardio-dental syndrome: a case report
• A novel deletion mutation, c.1296delT in the BCOR gene, is associated with oculo-facio-cardio-dental syndrome
• A potential molecular pathogenesis of cardiac/laterality defects in Oculo-Facio-Cardio-Dental syndrome
• A Rare Case of Nonsyndromic Generalized Radiculomegaly with a Literature Review
• A Rare Case of Oculofaciocardiodental Syndrome
• A rare genotype of biallelic mosaic variants in BCOR gene causing a bilateral ocular anterior segment dysgenesis and cataracts
• A rare syndrome with unusual dental findings: Oculo-facio-cardio-dental syndrome
• Bcl6a function is required during optic cup formation to prevent p53-dependent apoptosis and colobomata
• BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects
• BCOR gene alterations in hematologic diseases
• BCOR mutations and unstoppable root growth: a commentary on oculofaciocardiodental syndrome: novel BCOR mutations and expression in dental cells
• BCOR regulates mesenchymal stem cell function by epigenetic mechanisms
• BCOR variants are associated with X-linked recessive partial epilepsy
• Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs*6) in <em>BCOR</em> Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing
• Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs*6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing
• Case reports of oculofaciocardiodental syndrome with unusual dental findings
• Characterization of Bcor expression in mouse development
• Clarifying the impact of polycomb complex component disruption in human cancers
• Congenital cataracts in females caused by BCOR mutations; report of six further families demonstrating clinical variability and diverse genetic mechanisms
• Dental management of a patient with oculo-facio-cardio-dental syndrome
• Endodontic management in oculo-facio-cardio-dental syndrome: a case report
• Evidence of Germline Mosaicism for a Novel BCOR Mutation in Two Indian Sisters with Oculo-Facio-Cardio-Dental Syndrome
• Expanding the phenotype of the X-linked BCOR microphthalmia syndromes
• Expression of Normal or Mutated X-Linked <em>BCOR</em> Transcripts in OFCD iPSCs
• Eye development genes and known syndromes
• Foveal photoreceptor atrophy, persistent fetal vasculature, congenital cataracts, and microphthalmia in a pediatric patient with <em>BCOR</em>-associated oculo-facio-cardio-dental (OFCD) syndrome
• Function analysis of mesenchymal Bcor in tooth development by using RNA interference
• Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition
• Giant canine with dentine anomalies in oculo-facio-cardio-dental syndrome
• Human Genetics of Ventricular Septal Defect
• Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis
• Identification of nuclear localization signals within the human BCOR protein
• Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determination
• Main genetic entities associated with supernumerary teeth
• Molecular characterization of co-occurring Duchenne muscular dystrophy and X-linked oculo-facio-cardio-dental syndrome in a girl
• Molecular mechanism of hyperactive tooth root formation in oculo-facio-cardio-dental syndrome
• Multiple pancreatic neuroendocrine tumors in OFCD syndrome caused by somatic BCOR mosaicism
• New radiological findings and radiculomegaly in oculofaciocardiodental syndrome with a novel BCOR mutation: A case report
• Nonsense-mediated mRNA decay affects hyperactive root formation in oculo-facio-cardio-dental syndrome via up-frameshift protein 1
• Nonsyndromic Generalized Radiculomegaly of Permanent Dentition: A Rare Case Report
• Novel BCOR mutation in a boy with Lenz microphthalmia/oculo-facio-cardio-dental (OFCD) syndrome
• Novel BCOR mutations in patients with oculofaciocardiodental (OFCD) syndrome
• Novel mutations in BCOR in three patients with oculo-facio-cardio-dental syndrome, but none in Lenz microphthalmia syndrome
• Nuclear import of transcriptional corepressor BCOR occurs through interaction with karyopherin α expressed in human periodontal ligament
• Ocular findings in a patient with oculofaciocardiodental (OFCD) syndrome and a novel BCOR pathogenic variant
• Ocular severe involvement in oculofaciocardiodental syndrome: Description of a case series
• Oculo-facio-cardio Dental Syndrome
• Oculo-facio-cardio-dental (OFCD) syndrome
• Oculo-facio-cardio-dental (OFCD) syndrome
• Oculo-facio-cardio-dental (OFCD) syndrome
• Oculo-facio-cardio-dental (OFCD) syndrome: a case report
• Oculo-facio-cardio-dental (OFCD) syndrome: the first Italian case of BCOR and co-occurring OTC gene deletion
• Oculo-facio-cardio-dental syndrome
• Oculo-facio-cardio-dental syndrome caused by <em>BCOR</em> gene mutations: a case report
• Oculo-facio-cardio-dental syndrome in a girl and her mother
• Oculo-facio-cardio-dental syndrome in a mother and daughter
• Oculo-facio-cardio-dental syndrome in three succeeding generations: genotypic data and phenotypic features
• Oculo-facio-cardio-dental syndrome with craniosynostosis, temporal hypertrichosis, and deafness
• Oculo-Facio-Cardio-Dental Syndrome: A Case Report about a Rare Pathological Condition
• Oculo-facio-cardio-dental syndrome: report of a rare case
• Oculo-facio-cardio-dental syndrome: skewed X chromosome inactivation in mother and daughter suggest X-linked dominant Inheritance
• Oculo-facio-cardio-dental syndrome: two new cases
• Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR
• Oculofaciocardiodental syndrome and orthodontics
• Oculofaciocardiodental syndrome caused by a novel BCOR variant
• Oculofaciocardiodental syndrome: a rare case and review of the literature
• Oculofaciocardiodental syndrome: novel BCOR mutations and expression in dental cells
• Oculofaciocardiodental syndrome: novel BCOR mutations and expression in dental cells
• Oculofaciocardiodental syndrome: report of a rare case
• OFCD syndrome and extraembryonic defects are revealed by conditional mutation of the Polycomb-group repressive complex 1.1 (PRC1.1) gene BCOR
• Oligodontia in the Clinical Spectrum of Syndromes: A Systematic Review
• Orthodontic treatment of a transposed gigantic canine --a case report
• Otodental syndrome, oculo-facio-cardio-dental (OFCD) syndrome, and lobodontia: dental disorders of interest to the pediatric radiologist
• Pancreatic endocrine microadenomatosis in a patient with oculofaciocardiodental (OFCD) syndrome
• Patient with oculo-facio-cardio-dental syndrome treated with surgical orthodontics
• Polycomb group and SCF ubiquitin ligases are found in a novel BCOR complex that is recruited to BCL6 targets
• Radiculomegaly of canines in oculofaciocardiodental syndrome
• Radiculomegaly of permanent canines: report of endodontic treatment in OFCD syndrome
• Radiculomegaly: a case report of this rare dental finding with review of the associated oculo-facio-cardio-dental syndrome
• Rare dental abnormalities seen in oculo-facio-cardio-dental (OFCD) syndrome: three new cases and review of nine patients
• Review Recent progress in identification and characterization of loci associated with sex-linked congenital cataract
• Role of the transcriptional corepressor Bcor in embryonic stem cell differentiation and early embryonic development
• Syndromes with supernumerary teeth
• Three cases of oculo-facio-cardio-dental (OFCD) syndrome
• Two Cases of Oculofaciocardiodental (OFCD) Syndrome due to X-Linked BCOR Mutations Presenting with Infantile Hemangiomas: Phenotypic Overlap with PHACE Syndrome
• Whole-exome sequencing identifies somatic mutations of BCOR in acute myeloid leukemia with normal karyotype