Application of Deafness Diagnostic Screening Panel Based on Deafness Mutation/Gene Database Using Invader Assay
Author:
Affiliation:
1. Division of Advanced Technology and Development, BML, Inc., Kawagoe-shi, Saitama 350-1101, Japan.
2. Department of Otorhinolaryngology, Shinshu University School of Medicine, Matsumoto 390-8621, Japan.
Publisher
Mary Ann Liebert Inc
Subject
Genetics(clinical)
Link
http://www.liebertpub.com/doi/pdf/10.1089/gte.2007.0002
Reference21 articles.
1. Three Familial Cases of Hearing Loss Associated with Enlargement of the Vestibular Aqueduct
2. GJB2: The spectrum of deafness-causing allele variants and their phenotype
3. A genotype-phenotype correlation for GJB2 (connexin 26) deafness
4. Invader technology for DNA and RNA analysis: principles and applications
5. Heteroplasmy for the 1555A>G mutation in the mitochondrial 12S rRNA gene in six Spanish families with non-syndromic hearing loss
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