Orzan, E <br/><br/>
Molecular genetics applied to clinical practice: the Cx26 hearing impairment.  [electronic resource] 

 -  British journal of audiology  Oct 1999 
 - 291-5 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0300-5364 
<br/><br/><label>Standard No.: </label>10.3109/03005369909090112  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Alleles<br/>Audiology<br/>Audiometry, Pure-Tone--methods<br/>Child<br/>Child, Preschool<br/>Chromosome Aberrations--genetics<br/>Chromosome Disorders<br/>Connexin 26<br/>Connexins<br/>Gene Expression--genetics<br/>Health Services<br/>Hearing Loss, Sensorineural--diagnosis<br/>Humans<br/>Molecular Biology--methods<br/>Point Mutation--genetics<br/>Retrospective Studies<br/>Severity of Illness Index