Research Studies Archive
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
Distinguishing 3 classes of corpus callosal abnormalities in consanguineous families
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
Agenesis of the corpus callosum associated with narcolepsy-cataplexy
Demographic, ocular and associated neurological findings in corpus callosum malformations
Prenatal Imaging Features and Postnatal Outcome of Short Corpus Callosum: A Series of 42 Cases
Prenatal genetic testing in 19 fetuses with corpus callosum abnormality
On the outside looking in: a phenomenological study of the lived experience of Australian adu
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