Lezirovitz, Karina <br/><br/>
Is autosomal recessive deafness associated with oculocutaneous albinism a "coincidence syndrome"?  [electronic resource] 

 -  Journal of human genetics  2006 
 - 716-720 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1434-5161 
<br/><br/><label>Standard No.: </label>10.1007/s10038-006-0003-7  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Albinism, Oculocutaneous--complications<br/>Antigens, Neoplasm<br/>Audiometry, Pure-Tone<br/>Child<br/>Child, Preschool<br/>Connexin 26<br/>Connexins<br/>DNA Mutational Analysis<br/>Deafness--complications<br/>Exons--genetics<br/>Female<br/>Genes, Recessive--genetics<br/>Haplotypes<br/>Heterozygote<br/>Humans<br/>Male<br/>Membrane Proteins--genetics<br/>Membrane Transport Proteins<br/>Molecular Sequence Data<br/>Pedigree<br/>Syndrome