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Concurrent Hearing and Genetic Screening of 18 001 Neonates with Hearing Diagnose in Nantong, China

2021-04-19

Abstract excerpt

<h4>Objectives: </h4> Concurrent hearing and genetic screening of newborns is expected to play an important role in the early detection and diagnosis of congenital deafness, which triggers an intervention, as well as in predicting late-onset and progressive hearing loss and identifying individuals who are at risk of drug-induced hearing loss (HL). <h4>Methods: </h4> A Deafness Gene Variant Detection Array Kit cove...

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Literature Corpus work
6fc04cfa-25fa-53e1-9b04-4da995290714
DOI
10.21203/rs.3.rs-404100/v1
Open publication

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Concurrent Hearing and Genetic Screening of 18 001 Neonates with Hearing Diagnose in Nantong, ChinaDOI 10.21203/rs.3.rs-404100/v1
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