Research Studies Archive
Agenesis of the corpus callosum: an MR imaging analysis of associated abnormalities in the fetus
Agenesis of the corpus callosum in California 1983-2003: a population-based study
Mapping of deletion and translocation breakpoints in 1q44 implicates the serine/threonine kinase AKT3 in postnatal microcephaly and agenesis of the corpus callosum
Agenesis of the corpus callosum, optic coloboma, intractable seizures, craniofacial and skeletal dysmorphisms: an autosomal recessive disorder similar to Temtamy syndrome
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
DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome
Astroglial-Mediated Remodeling of the Interhemispheric Midline Is Required for the Formation of the Corpus Callosum
Reply: ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability
A de novo mutation in PRICKLE1 in fetal agenesis of the corpus callosum and polymicrogyria
Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes
Newsletter Sign Up
Sign up for our newsletter to receive the latest updates, research highlights, community stories, and upcoming events. Stay informed and connected with the DCC community—delivered straight to your inbox!
"*" indicates required fields
