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D Y Han

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Clinical Genetics|September 18, 2007
A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese familyJ Cheng, D Y Han, P Dai, et al.
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Showing results (51-60 of 51) with videos related to

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Pageof 6
You have reached the last page of results.This site can display upto 51 results.
Clinical Genetics|September 18, 2007
A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late-onset non-syndromic hearing loss in a Chinese familyJ Cheng, D Y Han, P Dai, et al.
Pageof 6