Trabelsi, Mediha <br/><br/>
GJB2 and GJB6 screening in Tunisian patients with autosomal recessive deafness.  [electronic resource] 

 -  International journal of pediatric otorhinolaryngology  May 2013 
 - 714-6 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1872-8464 
<br/><br/><label>Standard No.: </label>10.1016/j.ijporl.2013.01.024  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>Connexin 26<br/>Connexin 30<br/>Connexins--genetics<br/>Deafness--genetics<br/>Female<br/>Genes, Recessive<br/>Genetic Testing<br/>Hearing Loss, Sensorineural--genetics<br/>Humans<br/>Male<br/>Mass Screening<br/>Mutation<br/>Polymerase Chain Reaction<br/>Prevalence<br/>Sequence Analysis, DNA<br/>Tunisia<br/>Young Adult