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Browsing by Author Meyer, N.C.
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Issue Date
Title
Author(s)
2011
DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss
Hildebrand, M.S.
;
Morin, M.
;
Meyer, N.C.
;
Mayo, F.
;
Modamio-Hoybjor, S.
, et al
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