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Showing results 45 to 64 of 73 < previous next >

Title	Author(s)	Issue Date	Views
Monoallelic Mutations in CC2D1A Suggest a Novel Role in Human Heterotaxy and Ciliary Dysfunction Journal:Circulation: Genomic and Precision Medicine	Ma, ACH Mak, CCY Yeung, KS Pei, LCS Ying, D YU, HC Hasan, KMM Chen, X Chow, PC Cheung, YF Chung, BHY	2020	7
Muddling Through Muscle Genes – The Quest For Diagnosis In 50 Patients With Neuromuscular Disorders Using Whole Exome Sequencing. Proceeding/Conference:Asian Oceanian Congress of Child Neurology	Tsang, MHY Chiu, ATG Kwong, BMH Rui, LIANG Yu, MHC Yeung, KS Ho, WHL Mak, CCY Leung, GKC Muntoni, F Chung, BHY Chan, HSS	2019	27
Mutation in PIK3CA leading to developmental mosaic disorders Proceeding/Conference:Annual Scientific Meeting of the Hong Kong College of Paediatricians, HKCPaed 2015	Yeung, KS Leung, GKC Wong, WL Li, CH Choi, KY Kuong, EEYL Chow, W To, MKT Ip, JKJ Chow, CP Chan, GCF Chung, BHY	2015	155
Next generation sequencing in prenatal diagnosis Proceeding/Conference:American Society of Human Genetics Annual Meeting, ASHG2017	Leung, GKC Mak, CCY Pei, SLC Tsang, MHY Yu, MHC Yeung, KS Mok, GTK Hui, APW Tang, MHY Chan, KYK Kan, SYA Chung, BHY	2017	59
Novel damaging mutations in CC2D1A suggest a role in human heterotaxy and ciliary dysfunction Proceeding/Conference:American Society of Human Genetics (ASHG) Virtual Meeting, 2020	Chung, BHY Ma, ACH Mak, CCY Yeung, KS Ding, J Pei, LCS Ying, D Chow, PC Yu, HC Hasan, KMM Chen, X Cheung, YF	2020	11
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	Chan, SC Yeung, KS	2003	116
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	Pun, CKS Chan, SC Yeung, KS Ho, KL	2002	158
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	Chan, SC Carson Pun, KS Yeung, KS Ho, KL	2002	201
On the Design and Multiplier-less Realization of Digital IF for software radio Receivers Proceeding/Conference:Proc. European Signal Processing Conference (EUSIPCO2002)	Yeung, KS Chan, SC	2002	102
On the design and multiplier-less realization of digital IF for software radio receivers with prescribed output accuracy	Chan, SC Yeung, KS	2002	116
On the design and multiplierless realization of perfect reconstruction triplet-based FIR filter banks and wavelet bases Journal:IEEE Transactions on Circuits and Systems I: Regular Papers	Chan, SC Yeung, KS	2004	163
On the minimax design of passband linear-phase variable digital filters using semidefinite programming Journal:IEEE Signal Processing Letters	Tsui, KM Yeung, KS Chan, SC Tse, KW	2004	184
Paternal uniparental disomy of chromosome 19 in a pair of monochorionic diamniotic twins with dysmorphic features and developmental delay Journal:Journal of Medical Genetics	Yeung, KS Ho, SP Lee, SL Kan, SYA Chan, YK Tang, MHY MAK, CCY Leung, KC So, PL Pfundt, R Marshall, CR Scherer, SW Choufani, S Weksberg, R Chung, BHY	2018	67
Prenatal and postnatal diagnosis of Schuurs‐Hoeijmakers syndrome: Case series and review of the literature Journal:American Journal of Medical Genetics Part A	Seto, TYM Bertoli-Avella, AM Cheung, KW Chan, YK Yeung, KS Fung, LF Beetz, C Bauer, P Luk, HM Lo, FMI Lee, CP Chung, BHY Kan, SYA	2020	6
Primary coenzyme Q10 deficiency-7: expanded phenotypic spectrum and a founder mutation in southern Chinese Journal:npj Genomic Medicine	YU, MHC TSANG, MHY Lai, S Ho, MSP Tse, DML Willis, B Kwong, AKY Chou, YY Lin, SP Quinzii, CM Hwu, WL Chien, YH Kuo, PL Chan, VCM Tsoi, C Chong, SC Rodenburg, RJT Smetinik, J Mak, CCY Yeung, KS Fung, LF Lam, W Hui, J Lee, NC Fung, CW Chung, BHY	2019	52
Rare SUZ12 variants commonly cause an overgrowth phenotype Journal:American Journal of Medical Genetics Part C: Seminars in Medical Genetics	Cyrus, SS Cohen, ASA Agbahovbe, R Avela, K Yeung, KS Chung, BHY Luk, HM Tkachenko, N Choufani, S Weksberg, R Lopez-Rangel, E Brown, K Sanenz, MS Svihovec, S McCandless, SE Bird, LM Garcia, AG Cambello, MJ McWalter, K Schnur, RE An, J Jones, SJM Bhalla, SK Pinz, H Braddock, SR Gibson, WT	2019	17
Reading NGS Test Report: What a clinician needs to know Proceeding/Conference:HA 2016 Commissioned Training Programme - Genetics in O&G	Chung, BHY Leung, KC Yeung, KS Mak, CCY	2016	29
Retrospective cohort analysis on couples seeking pre-implantation genetic testing over a 5-year period 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)	Fung, JLF Chan, KLS Yeung, KS Lee, M Chow, JFC Li, RHW Ng, EHY Chung, BHY	2020	10
Silver-Russell syndrome in Hong Kong Journal:Hong Kong Medical Journal	Luk, HM YEUNG, KS Wong, WL Chung, BHY Tong, TMF Lo, IFM	2016	60
Somatic mosaicism of PIK3CA mutation in PIK3CA-related overgrowth disorders Proceeding/Conference:Annual Scientific Meeting of the Hong Kong College of Paediatricians, HKCPaed 2014	Yeung, KS Leung, KC Wong, WL Li, RCH Choi, KY Kuong, EYL Chow, W To, M Chan, GCF Chung, BHY	2014	104

Showing results 45 to 64 of 73 < previous next >