Browsing by Author YEUNG, KS

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TitleAuthor(s)Issue DateViews
 
2014
85
2015
66
 
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
58
 
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
39
 
Identification of epigenetic alterations in imprinting growth disorders
Proceeding/Conference:HKU Department of Paediatrics & Adolescent Medicine Golden Jubilee Scientific Meeting
2014
59
 
2017
46
 
2018
53
 
Mutation in PIK3CA leading to developmental mosaic disorders
Proceeding/Conference:Annual Scientific Meeting of the Hong Kong College of Paediatricians, HKCPaed 2015
2015
88
 
Next generation sequencing in prenatal diagnosis
Proceeding/Conference:American Society of Human Genetics Annual Meeting, ASHG2017
2017
45
On the application of variable digital filters (VDF) to the realization of software radio receivers
Proceeding/Conference:Proceedings - IEEE International Symposium on Circuits and Systems
2003
61
 
On the design and implementation of FIR and IIR digital filters with variable frequency characteristics
Journal:IEEE Transactions on Circuits and Systems II: Analog and Digital Signal Processing
2002
67
 
On the design and implementation of FIR and IIR digital filters with variable frequency characteristics
Proceeding/Conference:IEEE International Symposium on Circuits and Systems Proceedings
2002
112
 
On the Design and Multiplier-less Realization of Digital IF for software radio Receivers
Proceeding/Conference:Proc. European Signal Processing Conference (EUSIPCO2002)
2002
45
 
2002
40
 
2004
56
 
2004
67
 
2018
45
 
Reading NGS Test Report: What a clinician needs to know
Proceeding/Conference:HA 2016 Commissioned Training Programme - Genetics in O&G
2016
22
 
Silver-Russell syndrome in Hong Kong
Journal:Hong Kong Medical Journal
2016
24
 
Somatic mosaicism of PIK3CA mutation in PIK3CA-related overgrowth disorders
Proceeding/Conference:Annual Scientific Meeting of the Hong Kong College of Paediatricians, HKCPaed 2014
2014
103