DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23. [electronic resource]
Producer: 20040223Description: 832-6 p. digitalISSN:- 1468-6244
- Adolescent
- Child
- Chromosomes, Human, Pair 1 -- genetics
- Female
- Genes, Dominant -- genetics
- Genes, Recessive -- genetics
- Genetic Linkage
- Genetic Markers -- genetics
- Haplotypes -- genetics
- Hearing Loss, Bilateral -- diagnosis
- Hearing Loss, Sensorineural -- diagnosis
- Humans
- Male
- Pedigree
- Physical Chromosome Mapping -- methods
- Spain
- Syndrome
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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