Martin, D M <br/><br/>
Characterisation and genetic mapping of a new X linked deafness syndrome.  [electronic resource] 

 -  Journal of medical genetics  Nov 2000 
 - 836-41 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.37.11.836  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Child<br/>Chromosome Banding<br/>Chromosome Mapping<br/>Family Health<br/>Female<br/>Genetic Linkage<br/>Haplotypes<br/>Hearing Loss, Sensorineural--genetics<br/>Humans<br/>Male<br/>Middle Aged<br/>Pedigree<br/>Syndrome<br/>X Chromosome--genetics