Sensorineural hearing impairment, non-syndromic: DFNB5, 6, 7. Homozygosity mapping to localize genes causing autosomal recessive non-syndromic hearing loss

Book chapter

Peer reviewed

K Fukushima, Y Ueki and R J Smith

Genetics in Otorhinolaryngology, Vol.56, pp.152-157

Advances in oto-rhino-laryngology, 56, Karger

2000

DOI: 10.1159/000059103

PMID: 10868227

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Review | No abstract available

Homozygote

Deafness - genetics

Humans

Chromosomes, Human, Pair 14

Chromosome Mapping

Hearing Loss, Sensorineural - genetics

Chromosomes, Human, Pair 9

Chromosomes, Human, Pair 7

Genes, Recessive

Title: Subtitle: Sensorineural hearing impairment, non-syndromic: DFNB5, 6, 7. Homozygosity mapping to localize genes causing autosomal recessive non-syndromic hearing loss
Creators: K Fukushima - Department of Otolaryngology, Okayama University Medical School, Japan. kuni@cc.okayama-u.ac.jp
Y Ueki
R J Smith
Resource Type: Book chapter
Publication Details: Genetics in Otorhinolaryngology, Vol.56, pp.152-157
Series: Advances in oto-rhino-laryngology; 56
DOI: 10.1159/000059103
PMID: 10868227
NLM abbreviation: Adv Otorhinolaryngol
ISSN: 0065-3071
eISSN: 1662-2847
Publisher: Karger; Basel
Grant note: 1RO1 DC02842 / NIDCD NIH HHS
Language: English
Date published: 2000
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: 9984006411202771

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