Pfister, M <br/><br/>
DFN4: non-syndromic autosomal dominant X-linked sensorineural hearing impairment.  [electronic resource] 

 -  Advances in oto-rhino-laryngology  2000 
 - 196-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Review 
<br/><br/><label>ISSN: </label>0065-3071 
<br/><br/><label>Standard No.: </label>10.1159/000059102  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Mapping<br/>Deafness--genetics<br/>Dystrophin--genetics<br/>Female<br/>Genes, Dominant<br/>Hearing Loss, Sensorineural--genetics<br/>Humans<br/>Male<br/>Muscular Dystrophy, Duchenne--genetics<br/>X Chromosome