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Dissecting the regulatory architecture of gene expression QTLs.
Clinical and molecular diagnosis of Miller-Dieker syndrome.
Direct observation in medical education: a review of the literature and evidence for validity.
Cystoid macular edema associated with fingolimod use for multiple sclerosis.
Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene.
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Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene.
Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene. Brain. 2013 Nov; 136(Pt 11):3378-94.
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PubMed
subject areas
Abnormalities, Multiple
Adolescent
Adult
Animals
Brain
Child
Chromosome Deletion
Chromosomes, Human, Pair 6
Cohort Studies
Developmental Disabilities
Epilepsy
Exome
Female
Haploinsufficiency
Humans
Infant
Magnetic Resonance Imaging
Male
Malformations of Cortical Development, Group II
Mutation
Periventricular Nodular Heterotopia
Rats
Rats, Wistar
Syndrome
authors with profiles
William B. Dobyns