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Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2.
Autosomal recessive mutations in nuclear transport factor KPNA7 are associated with infantile spasms and cerebellar malformation.
Sleep, off-line processing, and vocal learning.
A study of functional anatomy of aortic-mitral valve coupling using 3D matrix transesophageal echocardiography.
Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients.
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Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients.
Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients. Brain. 2010 May; 133(Pt 5):1415-27.
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PubMed
subject areas
Age of Onset
Child, Preschool
Cohort Studies
Developmental Disabilities
Epilepsy
Female
Humans
Infant
Infant, Newborn
Magnetic Resonance Imaging
Male
Malformations of Cortical Development
Microcephaly
Muscle Spasticity
Prevalence
Sex Distribution
authors with profiles
William B. Dobyns