de Brouwer, Arjan P M <br/><br/>
Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1-22.3.  [electronic resource] 

 -  American journal of medical genetics. Part A  Aug 2005 
 - 41-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.30844  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 6--genetics<br/>Family Health<br/>Female<br/>Genes, Dominant<br/>Genetic Markers<br/>Genetic Predisposition to Disease--genetics<br/>Hearing Loss--genetics<br/>Humans<br/>Lod Score<br/>Male<br/>Pedigree