Chattaraj, Parna <br/><br/>
A common   [electronic resource] 

 -  Journal of medical genetics  10 2017 
 - 665-673 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Intramural 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmedgenet-2017-104721  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Child<br/>Chromosomes, Human, Pair 7--genetics<br/>Cohort Studies<br/>Female<br/>Genetic Variation<br/>Genotype<br/>Haplotypes<br/>Hearing Loss, Sensorineural--genetics<br/>Heterozygote<br/>Humans<br/>Male<br/>Membrane Transport Proteins--genetics<br/>Microsatellite Repeats<br/>Sequence Analysis, DNA<br/>Sulfate Transporters<br/>Vestibular Aqueduct--abnormalities