Al-Achkar, Walid <br/><br/>
First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss.  [electronic resource] 

 -  International journal of pediatric otorhinolaryngology  Jan 2017 
 - 82-87 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.2016.11.015  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Connexin 26<br/>Connexin 30<br/>Connexins--genetics<br/>Exons<br/>Female<br/>Genotype<br/>Hearing Loss, Sensorineural--genetics<br/>Heterozygote<br/>Humans<br/>Male<br/>Multiplex Polymerase Chain Reaction<br/>Mutation<br/>Polymerase Chain Reaction<br/>Polymorphism, Restriction Fragment Length<br/>Sequence Deletion<br/>Syria