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Mapping a new autosomal dominant hearing loss locus, DFNA20, ON 17Q25 and searching for the disease causing gene(s)
Wei, Sainan
Text (2002)
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Electronic Theses & Dissertations
Mapping, mutation identification and expression study of DFNB3, a gene for human recessive deafnes [i.e. deafness]
Liang, Yong
Text (1999)
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