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Molecular Diagnosis of Hearing Loss

  • Published:2012-01 Issue:1 Volume:72 Page:
  • ISSN:1934-8266
  • Container-title:Current Protocols in Human Genetics
  • language:en
  • Short-container-title:Current Protocols in Human Genetics

Author:

Brown Kerry K.12,Rehm Heidi L.13

Affiliation:

1. Department of Pathology, Brigham and Women's Hospital Boston Massachusetts

2. Department of Genetics, Harvard Medical School Boston Massachusetts

3. Laboratory for Molecular Medicine, Partners Healthcare Center for Personalized Genetic Medicine Cambridge Massachusetts

Publisher

Wiley

Subject

General Medicine

Reference51 articles.

1. 1000 Genomes Project:http://www.1000genomes.org/. Accessed:2011.

2. Genetics evaluation guidelines for the etiologic diagnosis of congenital hearing loss;ACMG, Genetics evaluation of congenital hearing loss expert panel;Genet Med.,2002

3. Genotype–phenotype correlations for SLC26A4-related deafness

4. Ballana E. Ventayol M. Rabionet R. Gasparini P. andEstivill X.2011. Connexins and deafness homepage:http://www.crg.es/deafness. Accessed: 2011.

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