Macrocerebellum, epilepsy, intellectual disability, and gut malrotation in a child with a 16q24.1-q24.2 contiguous gene deletion. [electronic resource]
Producer: 20150331Description: 2062-8 p. digitalISSN:- 1552-4833
- Abnormalities, Multiple -- diagnosis
- Cerebellum -- abnormalities
- Child, Preschool
- Chromosome Deletion
- Chromosome Mapping
- Chromosomes, Human, Pair 16
- Epilepsy -- genetics
- Female
- Genetic Association Studies
- Humans
- In Situ Hybridization, Fluorescence
- Intellectual Disability -- diagnosis
- Magnetic Resonance Imaging
- Phenotype
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Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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