Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant gene. [electronic resource]
Producer: 19940909Description: 914-20 p. digitalISSN:- 0022-3050
- Adolescent
- Adult
- Cerebral Cortex -- abnormalities
- Child
- Congenital Abnormalities -- diagnosis
- Epilepsy -- etiology
- Female
- Genes, Dominant -- genetics
- Genetic Counseling
- Genetic Linkage -- genetics
- Humans
- Infant
- Intellectual Disability -- etiology
- Magnetic Resonance Imaging
- Male
- Pedigree
- Sex Chromosome Aberrations -- diagnosis
- X Chromosome
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Publication Type: Case Reports; Journal Article
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