Browsing by Author Ying, D

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TitleAuthor(s)Issue DateViews
 
2014
75
 
2017
28
 
2017
54
 
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
71
 
2015
25
 
2013
86
 
2016
12
 
2015
96
 
2010
187
 
2015
65
 
2015
70
 
2011
226
 
2014
64
2015
48
 
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
24
 
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
18
 
2017
3
 
2009
70
 
2013
186
 
2014
53