Nonsyndromic 35 delG mutation of the connexin 26 gene associated with deafness in syndromic children: two case reports.

The Laryngoscope

PubMedID: 15091236

Venail F, Roux AF, Pallares-Ruiz N, Claustres M, Blanchet P, Gardiner Q, Mondain M. Nonsyndromic 35 delG mutation of the connexin 26 gene associated with deafness in syndromic children: two case reports. Laryngoscope. 2004;114(3):566-9.
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