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Epilepsy and outcome in FOXG1-related disorders.
CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development.
Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1.
Reasons for nonadherence to guidelines for aortic valve replacement in patients with severe aortic stenosis and potential solutions.
A developmental and genetic classification for malformations of cortical development: update 2012.
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A developmental and genetic classification for malformations of cortical development: update 2012.
A developmental and genetic classification for malformations of cortical development: update 2012. Brain. 2012 May; 135(Pt 5):1348-69.
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PubMed
subject areas
Cell Movement
Cerebral Cortex
Developmental Disabilities
Diagnostic Imaging
Epilepsy
History, 21st Century
Humans
Malformations of Cortical Development
Molecular Biology
Mutation
authors with profiles
William B. Dobyns