Mustapha, Mirna <br/><br/>
A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25.  [electronic resource] 

 -  Human genetics  Apr 2002 
 - 348-50 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/s00439-002-0690-x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 17<br/>Female<br/>Genetic Linkage<br/>Hearing Loss, Sensorineural--genetics<br/>Humans<br/>Male<br/>Pedigree<br/>Retinitis Pigmentosa--genetics<br/>Syndrome