Moreno-Pelayo, M A <br/><br/>
DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23.  [electronic resource] 

 -  Journal of medical genetics  Nov 2003 
 - 832-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.40.11.832  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>Chromosomes, Human, Pair 1--genetics<br/>Female<br/>Genes, Dominant--genetics<br/>Genes, Recessive--genetics<br/>Genetic Linkage<br/>Genetic Markers--genetics<br/>Haplotypes--genetics<br/>Hearing Loss, Bilateral--diagnosis<br/>Hearing Loss, Sensorineural--diagnosis<br/>Humans<br/>Male<br/>Pedigree<br/>Physical Chromosome Mapping--methods<br/>Spain<br/>Syndrome