Linkage of internal minisatellite loci on chromosome 1 and exclusion of autosomal dominant retinitis pigmentosa proximal to rhesus.
case_report · Level V
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- Record sourced from PubMed, PMID 2106582.
- Also identified by PMC identifier 1016872.
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Abstract
We report the exclusion of a locus for autosomal dominant retinitis pigmentosa proximal to the rhesus locus in a single large pedigree. In addition, a previously unreported linkage is described between two chromosome 1 markers, which confirms that a highly variable minisatellite locus is placed internally on chromosome 1.
Medical subject headings
- Chromosomes, Human, Pair 1
- DNA, Satellite
- Retinitis Pigmentosa