Browsing by Author Ying, D

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TitleAuthor(s)Issue DateViews
 
2014
124
 
2017
97
 
2017
102
 
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
98
 
2015
56
 
2013
149
 
2016
44
 
2015
228
 
2010
309
 
2015
128
 
2015
119
 
2011
127
 
2014
98
2015
82
 
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
67
 
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
46
 
2017
59
 
2009
108
 
2013
211
 
2014
67