A child with deletion (14)(q24.3q32.13) and auditory neuropathy. [electronic resource]
Producer: 20080108Description: 117-23 p. digitalISSN:- 1552-4833
- Calmodulin -- genetics
- Cell Cycle Proteins -- genetics
- Child, Preschool
- Chromogranin A -- genetics
- Chromosome Breakage
- Chromosome Mapping
- Chromosomes, Human, Pair 14
- Female
- Forkhead Transcription Factors
- Gene Deletion
- Goosecoid Protein -- genetics
- Hearing Loss, Sensorineural -- diagnosis
- Humans
- In Situ Hybridization, Fluorescence
- Karyotyping
- Monomeric Clathrin Assembly Proteins -- genetics
- Multigene Family
- Repressor Proteins -- genetics
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Publication Type: Case Reports; Journal Article
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