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Allogeneic hematopoietic stem cell transplantation for lymphoma.
Single-cell sequencing reveals lineage-specific dynamic genetic regulation of gene expression during human cardiomyocyte differentiation.
Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion.
Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debre type.
Genotypically defined lissencephalies show distinct pathologies.
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Genotypically defined lissencephalies show distinct pathologies.
Genotypically defined lissencephalies show distinct pathologies. J Neuropathol Exp Neurol. 2005 Oct; 64(10):847-57.
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PubMed
subject areas
1-Alkyl-2-acetylglycerophosphocholine Esterase
Adolescent
Adult
Brain
Brain Diseases
Brain Stem
Cerebellum
Cerebral Cortex
Child
Child, Preschool
Choristoma
Congenital Abnormalities
Female
Genotype
Homeodomain Proteins
Humans
Infant
Infant, Newborn
Intellectual Disability
Male
Microtubule-Associated Proteins
Middle Aged
Mutation
Neuropeptides
Transcription Factors
authors with profiles
William B. Dobyns