Publication | Open Access

A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutations

Early DiagnosisDevelopmental BiologyNoninvasive Prenatal ScreeningAudiologyPediatricsHearing ScreeningPrenatal DiagnosisSlc26a4 MutationsEarly DetectionHuman HearingArtsMedicineQuantitative Csmart AssayHearing Loss