Forty-six genes causing nonsyndromic hearing impairment: Which ones should be analyzed in DNA diagnostics?

Author:

Hilgert Nele,Smith Richard J.H.,Van Camp Guy

Publisher

Elsevier BV

Subject

Health, Toxicology and Mutagenesis,Genetics

Reference47 articles.

1. Newborn hearing screening—a silent revolution;Morton;N. Engl. J. Med.,2006

2. Review and meta-analysis of the epidemiology of congenital cytomegalovirus (CMV) infection;Kenneson;Rev. Med. Virol.,2007

3. Nonsyndromic hearing impairment: unparalleled heterogeneity;Van Camp;Am. J. Hum. Genet.,1997

4. Hereditary Hearing Loss and its Syndromes;Toriello,2004

5. Deafness genes and their diagnostic applications;Cryns;Audiol. Neurootol.,2004

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