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Aortic valve anatomy and assessment by transesophageal echocardiography.
B cell antigen receptor signaling and internalization are mutually exclusive events.
Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment.
Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker-Warburg syndrome.
The evolution of compensation to herbivory in scarlet gilia, Ipomopsis aggregata: herbivore-imposed natural selection and the quantitative genetics of tolerance.
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Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment.
Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment. Ann Neurol. 2000 Jul; 48(1):39-48.
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subject areas
Adolescent
Adult
Aged
Brain Diseases
Cerebral Cortex
Child
Child, Preschool
Epilepsy
Female
Humans
Infant
Magnetic Resonance Imaging
Male
Middle Aged
Pedigree
authors with profiles
William B. Dobyns