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

Journal article

Peer reviewed

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

Annals of the New York Academy of Sciences, Vol.630(1), pp.298-300

1991

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

PMID: 1952612

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no abstract

Genetic Markers

DNA Probes

Deafness - genetics

Humans

Retinitis Pigmentosa - genetics

Chromosome Mapping

Chromosomes, Human, Pair 4

Deafness - diagnosis

Syndrome

Retinitis Pigmentosa - diagnosis

Retinitis Pigmentosa - classification

Deafness - classification

Genetic Linkage

Title: Subtitle: Report on attempts to localize Usher syndrome type 1 by linkage analysis to selected candidate regions
Creators: S Pieke Dahl - Center for Hereditary Communication Disorders, Boys Town National Research Hospital, Omaha, Nebraska 68131
M D Weston
W J Kimberling
J B Kenyon
Y Y Shugart
R J Smith
Resource Type: Journal article
Publication Details: Annals of the New York Academy of Sciences, Vol.630(1), pp.298-300
DOI: 10.1111/j.1749-6632.1991.tb19612.x
PMID: 1952612
NLM abbreviation: Ann N Y Acad Sci
ISSN: 0077-8923
eISSN: 1749-6632
Publisher: Blackwell Publishing Ltd; United States
Language: English
Date published: 1991
Academic Unit: Roy J. Carver Department of Biomedical Engineering; Molecular Physiology and Biophysics; Anatomy and Cell Biology; Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Otolaryngology; Internal Medicine
Record Identifier: 9984007190802771

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