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Combined Carrier Screening and Prenatal Diagnosis for Spinal Muscular Atrophy, Thalassemia and Hereditary Deafness in 2873 Chinese Pregnant Women

2022-09-30

Abstract excerpt

<h4>Purpose: </h4> To investigate the clinical significance of combined carrier screening and prenatal diagnosis for SMA, thalassemia and hereditary deafness. Methods There were 2873 pregnant women from Wenzhou Central Hospital in Wenzhou city Zhejiang Province, China, between February 2020 and January 2022 accepted carrier screening. Genomic DNA was extracted from saliva of the screened group. SMN1 exon 7 and/or...

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Literature Corpus work: 6d3c7156-14fe-5571-8f86-7fa8e8f1ba2e
DOI: 10.21203/rs.3.rs-2081415/v1

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