Cordblood-Based High-Throughput Screening for Deafness Gene of 646 Newborns in Jinan Area of China
Author:
Affiliation:
1. Department of Clinical Laboratory, Handan Central Hospital, Handan, China.
Publisher
Korean Society of Otorhinolaryngology-Head and Neck Surgery
Subject
Otorhinolaryngology,Surgery
Link
http://synapse.koreamed.org/pdf/10.3342/ceo.2015.8.3.211
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1. The genetic bases for non-syndromic hearing loss among Chinese
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4. A distinct spectrum of SLC26A4 mutations in patients with enlarged vestibular aqueduct in China
5. Mitochondrial deafness
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3. Combined hearing screening and genetic screening of deafness among Hakka newborns in China;International Journal of Pediatric Otorhinolaryngology;2020-09
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