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Dive into the research topics of 'Mutation analysis of SLC26A4 for Pendred syndrome and nonsyndromic hearing loss by high-resolution melting'. Together they form a unique fingerprint.- Sort by
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Neng Chen, Lisbeth Tranebjærg, Nanna Dahl Rendtorff, Iris Schrijver, Neng Chen, Lisbeth Tranebjærg, Nanna Dahl Rendtorff, Iris Schrijver