Report on attempts to localize Usher syndrome type 1 by linkage analysis to selected candidate regions

Ann N Y Acad Sci. 1991:630:298-300. doi: 10.1111/j.1749-6632.1991.tb19612.x.

Authors

S Pieke Dahl¹, M D Weston, W J Kimberling, J B Kenyon, Y Y Shugart, R J Smith

Affiliation

¹ Center for Hereditary Communication Disorders, Boys Town National Research Hospital, Omaha, Nebraska 68131.

PMID: 1952612
DOI: 10.1111/j.1749-6632.1991.tb19612.x

No abstract available

MeSH terms

Chromosome Mapping
Chromosomes, Human, Pair 4*
DNA Probes
Deafness / classification
Deafness / diagnosis
Deafness / genetics*
Genetic Linkage*
Genetic Markers
Humans
Retinitis Pigmentosa / classification
Retinitis Pigmentosa / diagnosis
Retinitis Pigmentosa / genetics*
Syndrome

Substances

DNA Probes
Genetic Markers