Van Laer, L <br/><br/>
A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment.  [electronic resource] 

 -  Journal of medical genetics  Aug 2001 
 - 515-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.38.8.515  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Connexin 26<br/>Connexins--genetics<br/>DNA--chemistry<br/>DNA Mutational Analysis<br/>Founder Effect<br/>Gene Frequency<br/>Genotype<br/>Hearing Loss, Sensorineural--genetics<br/>Humans<br/>Mutation<br/>Polymorphism, Single Nucleotide<br/>Sequence Deletion