Chen, Ying <br/><br/>
Development and validation of a fetal genotyping assay with potential for noninvasive prenatal diagnosis of hereditary hearing loss.  [electronic resource] 

 -  Prenatal diagnosis  Dec 2016 
 - 1233-1241 p.  digital 
<br/><br/> Publication Type: Journal Article; Validation Study 
<br/><br/><label>ISSN: </label>1097-0223 
<br/><br/><label>Standard No.: </label>10.1002/pd.4962  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Connexin 26--genetics<br/>Connexins--genetics<br/>DNA--blood<br/>Female<br/>Genetic Testing--methods<br/>Genotype<br/>Genotyping Techniques--methods<br/>Hearing Loss--congenital<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Infant, Newborn<br/>Membrane Transport Proteins--genetics<br/>Mutation<br/>Phenotype<br/>Pregnancy<br/>Prenatal Diagnosis--methods<br/>Sulfate Transporters