Browsing by Author Fung, CW

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 23 to 42 of 89 < previous   next >
TitleAuthor(s)Issue DateViews
 
2020
 
1999
109
 
1999
86
 
A diagrammatic approach to search for minimum sampling frequency and quantization resolution for digital control of power converters
Proceeding/Conference:PESC Record - IEEE Annual Power Electronics Specialists Conference
2007
148
 
2012
33
Dravet syndrome - genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children
Proceeding/Conference:Developmental Medicine and Child Neurology
2012
152
Dravet Syndrome-Genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children
Proceeding/Conference:International Meeting for Autism Research
2012
142
 
2018
83
 
2019
93
 
2011
217
 
2014
127
 
2017
53
 
2008
149
 
High diagnostic yield by whole exome sequencing in a cohort of patients with movement disorders and/or progressive spasticity – possible targeted treatment implications and a way to precison medicine
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
17
 
2012
82
 
Improving genetic diagnosis by whole exome sequencing in rare hereditary peripheral neuropathies
Proceeding/Conference:Hong Kong College of Paediatricians 4th Annual Scientific Meeting cum 5th HK-Guangdong-Shanghai-Chongquing Paediatric Exchange Meeting
2016
18
 
Infantile convulsion choreoathetosis syndrome in a Hong Kong Chinese family
Proceeding/Conference:Asian & Oceanian Epilepsy Congress, AOEC 2008
2008
146
 
Infantile Convulsion Choreoathetosis Syndrome in a Hong Kong Chinese Family
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2009
2009
157
 
Infantile convulsion choreoathetosis syndrome in a Hong Kong Chinese Family
Proceeding/Conference:ACGA-HKSMG 2008 International Conference
2008
126
 
International Paediatric Mitochondrial Disease Scale
Journal:Journal of Inherited Metabolic Disease
2016
39