Browsing by Author Ying, D

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TitleAuthor(s)Issue DateViews
 
2014
80
 
2017
33
 
2017
61
 
CFTR: I1023R is a rare but recurrent disease-causing mutation found in Chinese patients with cystic fibrosis
Proceeding/Conference:Annual Scientific Meeting of the Hong Kong College of Paediatricians, HKCPaed 2014
2014
74
 
2015
27
 
2013
89
 
2016
15
 
2015
100
 
2010
191
 
2015
67
 
2015
76
 
2011
229
 
2014
67
2015
52
 
Identification of a CFTR founder mutations, c.3068T>G:p.I1023R, which causes protein trafficking defects in Chinese patients with cystic fibrosis
Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016
2016
27
 
Identification of a novel homozygous missense mutation in ABR causing cerebellar hypoplasia with early lethality
Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016
2016
21
 
2017
13
 
2009
72
 
2013
190
 
2014
55