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Showing results 9 to 18 of 18 < previous

	Title	Author(s)	Issue Date
	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, SLC Ying, D YU, MHC Hasan, KMM Chen, X Chow, PC Cheung, YF Chung, BHY	2020
	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
	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
	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
	On the design and multiplier-less realization of digital IF for software radio receivers with prescribed output accuracy	Chan, SC Yeung, KS	2002
	Prenatal and postnatal diagnosis of Schuurs‐Hoeijmakers syndrome: Case series and review of the literature Journal:American Journal of Medical Genetics Part A	Seto, MTY Bertoli-Avella, AM Cheung, KW Chan, KYK Yeung, KS Fung, JLF Beetz, C Bauer, P Luk, HM Lo, IFM Lee, CP Chung, BHY Kan, ASY	2021
	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
	Somatic PIK3CA mutations in seven patients with PIK3CA-related overgrowth spectrum Journal:American Journal of Medical Genetics Part A	YEUNG, KS Ip, JKJ Chow, CP Kuong, EEYL Tam, PKH Chan, GCF Chung, BHY	2017
	The genetics of macrocephaly, autistic spectrum disorders and developmental delay in Chinese children Proceeding/Conference:Developmental Medicine and Child Neurology	Tso, WYW YEUNG, KS Ip, JKJ Liu, APY Lee, PPW Chu, WY Chong, CY Ho, MHK Chan, GCF Lau, YL Chung, BHY	2017
	The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes Journal:Molecular Genetics & Genomic Medicine	Yeung, KS Yu, FNY Fung, CW Wong, S Lee, HCH Fung, STH Fung, GPG Leung, KY Chung, WH Lee, YT Ng, VKS YU, HC Fung, JLF TSANG, MHY Chan, KYK Chan, SHS Kan, ASY Chung, BHY	2020

Showing results 9 to 18 of 18 < previous