Showing results 13 to 32 of 78
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| Title | Author(s) | Issue Date | Views | |
|---|---|---|---|---|
| 2018 | 72 | |||
| 2019 | ||||
CFTR founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosis Journal:Molecular Genetics & Genomic Medicine | 2017 | 110 | ||
Coexistence of paternally-inherited ABCC8 mutation and mosaic paternal uniparental disomy 11p hyperinsulinism Journal:International Journal of Pediatric Endocrinology | 2020 | |||
| 2022 | 12 | |||
Comprehensive genetic evaluation in paediatric-onset mitochondrial diseases 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 | |||
De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients Journal:npj Genomic Medicine | 2016 | 90 | ||
| 2020 | 24 | |||
Design and complexity optimization of a new digital IF for software radio receivers with prescribed output accuracy Journal:IEEE Transactions on Circuits and Systems I: Regular Papers | 2007 | 186 | ||
Design and implementation of multiplier-less tunable 2-D FIR filters using McClellan transformation Proceeding/Conference:Proceedings - IEEE International Symposium on Circuits and Systems | 2002 | |||
The design and multiplier-less realization of software radio receivers with reduced system delay Journal:IEEE Transactions on Circuits and Systems I: Regular Papers | 2004 | 173 | ||
Design of FIR digital filters with prescribed flatness and peak error constraints using second-order cone programming Journal:IEEE Transactions on Circuits and Systems II: Express Briefs | 2005 | 256 | ||
The design of two-channel prefect reconstruction FIR triplet wavelet filter banks using semidefinite programming Proceeding/Conference:Proceedings - IEEE International Symposium on Circuits and Systems | 2003 | 102 | ||
Detecting expansion of short tandem repeat in whole exome sequencing data of movement disorder cohort with bioinformatics tool expansion hunter Proceeding/Conference:Joint Annual Scientific Meeting 2020 of The Hong Kong Paediatric Society (HKPS), Hong Kong College of Paediatricians (HKCPaed), Hong Kong Paediatric Nurses Association (HKPNA) and Hong Kong College of Paediatric Nursing (HKCPN) | 2020 | 45 | ||
Diagnostic outcome of whole exome sequencing in Hong Kong familes with autism spectrum disorder 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 | 76 | ||
EHMT1 pathogenic variants and 9q34.3 microdeletions share altered DNA methylation patterns in patients with Kleefstra syndrome Journal:Journal of Translational Genetics and Genomics | 2020 | 46 | ||
Evaluating the clinical utility of genome sequencing for cytogenetically balanced chromosomal abnormalities in prenatal diagnosis Proceeding/Conference:Health Research Symposium 2021 | 2021 | |||
| 2021 | 44 | |||
Evaluating the diagnostgic impact and cost of rapid whole-exome sequencing for rare genetic diseases in Hong Kong 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 | |||
Evidence of spread of X Chromosome inactivation on Chromosome 15 in a girl with an Unbalanced t(X;15) Translocation Proceeding/Conference:Hong Kong Journal of Paediatrics (New series) | 2013 |