Bilateral polymicrogyria as the indicative feature in a child with a 22q11.2 deletion. [electronic resource]
Producer: 20110111Description: 344-6 p. digitalISSN:- 1878-0849
- Cerebral Cortex -- abnormalities
- Chromosome Deletion
- Chromosomes, Human, Pair 22
- Developmental Disabilities -- genetics
- DiGeorge Syndrome -- genetics
- Humans
- Infant
- Intellectual Disability -- genetics
- Magnetic Resonance Imaging
- Male
- Malformations of Cortical Development -- genetics
- Microcephaly -- genetics
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Publication Type: Case Reports; Journal Article
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