Browsing by Author Fung, CW

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TitleAuthor(s)Issue DateViews
 
2019
 
2020
 
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
 
2005
82
 
Two novel mutations of SMPD1 gene from a Chinese family with Niemann Pick Disease type A (NPD-A)
Proceeding/Conference:HKPS-HKPNA 2006 Joint Annual Scientific Meeting
2006
48
 
Two novel mutations of SMPD1 gene from a Chinese family with Niemann Pick Disease Type A (NPD-A)
Proceeding/Conference:50th Anniversary Symposium on Paediatric Neurology & Neuro-Rehabilitation
2005
38
 
2005
41
 
2002
59
 
2016
13
 
2017
30
 
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
37
 
Video-Fluoroscopic Study of Swallowing (VFSS) in Children with Neurological Disorders
Proceeding/Conference:International Congress of Pediatrics, IPA 2001
2001
57
 
Video-fluoroscopic Study of Swallowing (VFSS) in children with Neurological Disorders
Proceeding/Conference:Hong Kong Journal of Paediatrics (new series)
2004
54
 
2004