A new 1p36.13-1p36.12 microdeletion syndrome characterized by learning disability, behavioral abnormalities, and ptosis. [electronic resource]
Producer: 20210604Description: 927-932 p. digitalISSN:- 1399-0004
- Blepharoptosis -- genetics
- Calmodulin-Binding Proteins -- genetics
- CapZ Actin Capping Protein -- genetics
- Chromosome Deletion
- Chromosome Disorders -- genetics
- Chromosomes, Human, Pair 1 -- genetics
- Developmental Disabilities -- genetics
- Female
- Genetic Association Studies
- Humans
- Intellectual Disability -- genetics
- Learning Disabilities -- genetics
- Male
- Phenotype
- Ubiquitin-Protein Ligases -- genetics
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Publication Type: Journal Article
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