Browsing by Author YEUNG, KS

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TitleAuthor(s)Issue DateViews
 
2017
18
 
2014
41
 
2008
56
 
2016
29
 
1992
47
 
2017
22
 
The KLHL40C.1516A>C is a Chinese-specific founder mutation in causing nemaline myopathy 8
Proceeding/Conference:Joint Annual Scientific Meeting 2019, HK College of Paediatricians, 28 Sept 2019
2019
 
1993
56