Research Studies Archive
Anomalies of the corpus callosum: an MR analysis of the phenotypic spectrum of associated malformations
Genomic microarray analysis identifies candidate loci in patients with corpus callosum anomalies
Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance
Whole-exome sequencing identifies mutated c12orf57 in recessive corpus callosum hypoplasia
Distinguishing 3 classes of corpus callosal abnormalities in consanguineous families
Major brain malformations: corpus callosum dysgenesis, agenesis of septum pellucidum and polymicrogyria in patients with BCORL1-related disorders
Missense variants in DPYSL5 cause a neurodevelopmental disorder with corpus callosum agenesis and cerebellar abnormalities
De novo variants in SUPT16H cause neurodevelopmental disorders associated with corpus callosum abnormalities
Outcome of Rare Fetal Septal and Callosal Anomalies: A Systematic Review and Meta-Analysis
Demographic, ocular and associated neurological findings in corpus callosum malformations
Prenatal genetic testing in 19 fetuses with corpus callosum abnormality
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