Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation. [electronic resource]
Producer: 20051027Description: 1019-24 p. digitalISSN:- 1018-4813
- Adolescent
- Child
- Child, Preschool
- Chromosome Deletion
- Chromosomes, Human, Pair 22 -- genetics
- Female
- Humans
- In Situ Hybridization, Fluorescence
- Infant
- Intellectual Disability -- genetics
- Karyotyping
- Language Development Disorders -- genetics
- Male
- Molecular Biology
- Muscle Hypotonia
- Nucleic Acid Hybridization
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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