Genetic studies of Usher syndrome

Journal article

Peer reviewed

W J Kimberling, M D Weston, S Pieke Dahl, J B Kenyon, Y Y Shugart, C Moller, S L Davenport, A Martini, M Milani and R J Smith

Annals of the New York Academy of Sciences, Vol.630(1), pp.167-175

1991

DOI: 10.1111/j.1749-6632.1991.tb19585.x

PMID: 1952588

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no abstract

Family

DNA Probes

Chromosomes, Human, Pair 1

Deafness - genetics

Humans

Retinitis Pigmentosa - genetics

Adult

Chromosome Mapping

Ataxia - genetics

Syndrome

Intellectual Disability - genetics

Title: Subtitle: Genetic studies of Usher syndrome
Creators: W J Kimberling - Boys Town National Research Hospital, Omaha, Nebraska 68131
M D Weston
S Pieke Dahl
J B Kenyon
Y Y Shugart
C Moller
S L Davenport
A Martini
M Milani
R J Smith
Resource Type: Journal article
Publication Details: Annals of the New York Academy of Sciences, Vol.630(1), pp.167-175
DOI: 10.1111/j.1749-6632.1991.tb19585.x
PMID: 1952588
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: 9984007173902771

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