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Song learning and sleep.
Infantile cerebral and cerebellar atrophy is associated with a mutation in the MED17 subunit of the transcription preinitiation mediator complex.
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.
Band-like intracranial calcification with simplified gyration and polymicrogyria: a distinct "pseudo-TORCH" phenotype.
LIS1 missense mutations cause milder lissencephaly phenotypes including a child with normal IQ.
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LIS1 missense mutations cause milder lissencephaly phenotypes including a child with normal IQ.
LIS1 missense mutations cause milder lissencephaly phenotypes including a child with normal IQ. Neurology. 2001 Aug 14; 57(3):416-22.
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PubMed
subject areas
1-Alkyl-2-acetylglycerophosphocholine Esterase
Brain
Brain Diseases
Child
Child, Preschool
Female
Humans
Infant
Intelligence
Magnetic Resonance Imaging
Male
Microtubule-Associated Proteins
Mutation, Missense
Phenotype
authors with profiles
William B. Dobyns