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A de novo GRIN1 Variant Associated With Myoclonus and Developmental Delay: From Molecular Mechanism to Rescue Pharmacology.
Oculocerebrocutaneous syndrome: the brain malformation defines a core phenotype.
Cortical recruitment of centralspindlin and RhoA effectors during meiosis I of Caenorhabditiselegans primary spermatocytes.
A near miss: a nitrous oxide-carbon dioxide mix-up despite current safety standards.
Microlissencephaly: a heterogeneous malformation of cortical development.
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Microlissencephaly: a heterogeneous malformation of cortical development.
Microlissencephaly: a heterogeneous malformation of cortical development. Neuropediatrics. 1998 Jun; 29(3):113-9.
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PubMed
subject areas
Cerebral Cortex
Child, Preschool
Developmental Disabilities
Female
Humans
Infant
Infant, Newborn
Magnetic Resonance Imaging
Male
Microcephaly
Movement Disorders
Muscle Spasticity
Prognosis
Pyramidal Tracts
Retrospective Studies
Seizures
Terminology as Topic
authors with profiles
William B. Dobyns