Hearing loss in the nonocular Stickler syndrome caused by a COL11A2 mutation. [electronic resource]
Producer: 20000330Description: 457-61 p. digitalISSN:- 0023-852X
- Adult
- Age Factors
- Analysis of Variance
- Audiometry
- Auditory Threshold
- Bone Conduction -- genetics
- Chromosomes, Human, Pair 12 -- genetics
- Cleft Palate -- genetics
- Connective Tissue Diseases -- genetics
- Cross-Sectional Studies
- Disease Progression
- Female
- Genetic Linkage -- genetics
- Hearing Loss, Conductive -- genetics
- Hearing Loss, Sensorineural -- genetics
- Humans
- Linear Models
- Longitudinal Studies
- Male
- Middle Aged
- Mutation -- genetics
- Myopia -- genetics
- Otitis Media -- genetics
- Presbycusis -- genetics
- Prevalence
- Procollagen -- genetics
- Syndrome
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Publication Type: Journal Article
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