Yan, Denise <br/><br/>
Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing loss.  [electronic resource] 

 -  American journal of medical genetics. Part A  Feb 2007 
 - 385-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.31553  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosomes, Human, Pair 13<br/>Connexin 26<br/>Connexins--genetics<br/>Female<br/>Gene Frequency<br/>Hearing Loss--genetics<br/>Homozygote<br/>Humans<br/>Male<br/>Sequence Deletion<br/>Uniparental Disomy