Browsing by Author Kan, SYA

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing results 48 to 58 of 58 < previous 
TitleAuthor(s)Issue DateViews
 
2017
39
 
The KLHL40C.1516A>C is a Chinese-specific founder mutation in causing nemaline myopathy 8
Proceeding/Conference:Joint Annual Scientific Meeting 2019 of The Hong Kong Paediatric Society, Hong Kong College of Paediatricians, Hong Kong Paediatric Nurses Association, & Hong Kong College of Paediatric Nursing
2019
36
 
2017
167
 
Two unusual cases of haemoglobin Bart’s hydrops fetalis due to uniparental disomy or non-paternity.
Journal:Fetal Diagnosis and Therapy: clinical advances and basic research
2014
48
2013
108
 
2014
108
 
2016
45
 
Use of clinical chromosomal microarray in Hong Kong Chinese patients with autism spectrum disorder - implication of a copy number variation involving DPP10
Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016
2016
84
 
What is the Diagnosis?
Journal:Hong Kong Journal of Paediatrics (New series)
2016
37
 
2014
95
 
2017
25