The genetics of deafness-Reference-Cited by-同舟云学术

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The genetics of deafness

Published:2003 Issue:2 Volume:9 Page:109-119
ISSN:1080-4013
Container-title:Mental Retardation and Developmental Disabilities Research Reviews
language:en
Short-container-title:Ment. Retard. Dev. Disabil. Res. Rev.

Author:

Nance Walter E.

Publisher

Wiley

Subject

Genetics (clinical),Neuropsychology and Physiological Psychology,Pediatrics, Perinatology and Child Health

Reference55 articles.

1. A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family

2. Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss

3. Fine Mapping of the Human Biotinidase Gene and Haplotype Analysis of Five Common Mutations

4. Usher syndrome: Definition and estimate of prevalence from two high-risk populations

Cited by 179 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. Neuro‐Otology;Neurology;2024-03-15

2. The genetic basis and the diagnostic yield of genetic testing related to nonsyndromic hearing loss in Qatar;Scientific Reports;2024-02-20

3. Conductive and Sensorineural Hearing Loss;Textbook of Tinnitus;2024

4. Ear and Hearing Disorders;Avery's Diseases of the Newborn;2024

5. Parental knowledge and attitudes towards hereditary hearing loss and genetic technology;Electronic Journal of General Medicine;2023-11-01

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