Intragenic CAMTA1 deletions are associated with a spectrum of neurobehavioral phenotypes. [electronic resource]
Producer: 20160104Description: 478-82 p. digitalISSN:- 1399-0004
- Brain -- pathology
- Calcium-Binding Proteins -- genetics
- Child
- Chromosome Mapping
- Facies
- Female
- Genetic Association Studies
- Genetic Loci
- Genome-Wide Association Study
- Humans
- In Situ Hybridization, Fluorescence
- Magnetic Resonance Imaging
- Male
- Middle Aged
- Neurodevelopmental Disorders -- diagnosis
- Phenotype
- Sequence Deletion
- Trans-Activators -- genetics
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Publication Type: Case Reports; Journal Article
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