Phenotypic characterization of patients with early-onset high myopia due to mutations in [electronic resource]
Producer: 20181116Description: 560-573 p. digitalISSN:- 1090-0535
- Adolescent
- Adult
- Arthritis -- diagnosis
- Child
- Collagen Type II -- genetics
- Collagen Type XI -- genetics
- Connective Tissue Diseases -- diagnosis
- DNA Mutational Analysis
- Early Diagnosis
- Female
- Follow-Up Studies
- Genetic Association Studies
- Hearing Loss, Sensorineural -- diagnosis
- Humans
- Male
- Mutation
- Myopia, Degenerative -- diagnosis
- Pedigree
- Phenotype
- Retinal Detachment -- diagnosis
- Young Adult
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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