Molecular Diagnosis of Deafness: Impact of Gene Identification-Reference-Cited by-同舟云学术

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Molecular Diagnosis of Deafness: Impact of Gene Identification

Published:2002 Issue:3 Volume:7 Page:185-190
ISSN:1420-3030
Container-title:Audiology and Neurotology
language:en
Short-container-title:Audiol Neurotol

Author:

Usami Shin-ichi,Koda Eiko,Tsukamoto Koji,Otsuka Akihiro,Yuge Isamu,Asamura Kenji,Abe Satoko,Akita Jiro,Namba Atsushi

Publisher

S. Karger AG

Subject

Speech and Hearing,Sensory Systems,Otorhinolaryngology,Physiology

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A novel KCNQ4 one-base deletion in a large pedigree with hearing loss: implication for the genotype–phenotype correlation;Journal of Human Genetics;2006-04-05

2. Estimation of the frequency of occult mutations for an autosomal recessive disease in the presence of genetic heterogeneity: application to genetic hearing loss disorders;Human Mutation;2005-11

3. CT of the Ear in Pendred Syndrome;Radiology;2005-05

4. Hearing loss in patients with enlarged vestibular aqueduct: Air-bone gap and audiological Bing test;International Journal of Audiology;2005-01

5. Connexin 26 (GJB2) Gene-Related Deafness and Speech Intelligibility After Cochlear Implantation;Otology & Neurotology;2004-11

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