Assessment of the genetic causes of recessive childhood non-syndromic deafness in the UK - implications for genetic testing-Reference-Cited by-同舟云学术

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Assessment of the genetic causes of recessive childhood non-syndromic deafness in the UK - implications for genetic testing

Published:2005-11-10 Issue:6 Volume:68 Page:506-512
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Hutchin T,Coy NN,Conlon H,Telford E,Bromelow K,Blaydon D,Taylor G,Coghill E,Brown S,Trembath R,Liu XZ,Bitner-Glindzicz M,Mueller R

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2005.00539.x/fullpdf

Reference30 articles.

1. A critical review of the role of neonatal hearing screening in the detection of congenital hearing impairment;Davis;Health Technol Assess,1997

2. Van Camp G Smith RJH. http://www.webhost.ua.ac.be/hhh/

3. Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans;Zelante;Hum Mol Genet,1997

4. Connexin-26 mutations in sporadic non-syndromal sensorineural deafness;Lench;Lancet,1998

5. High carrier frequency of the 35delG deafness mutation in European populations. Genetic Analysis Consortium of GJB2 35delg;Gasparini;Eur J Hum Genet,2000

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