Weegerink, Nicole J D <br/><br/>
Phenotypes of two Dutch DFNA3 families with mutations in GJB2.  [electronic resource] 

 -  The Annals of otology, rhinology, and laryngology  Mar 2011 
 - 191-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0003-4894 
<br/><br/><label>Standard No.: </label>10.1177/000348941112000308  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution--genetics<br/>Audiometry, Pure-Tone<br/>Audiometry, Speech<br/>Child<br/>Connexin 26<br/>Connexins--genetics<br/>Female<br/>Hearing Loss, Sensorineural--genetics<br/>Humans<br/>Male<br/>Mutation, Missense<br/>Netherlands<br/>Phenotype<br/>Temporal Bone--diagnostic imaging<br/>Tomography, X-Ray Computed<br/>Vestibular Function Tests