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Showing results 1 to 15 of 15

	Title	Author(s)	Issue Date
	Automated method for the identification of conserved non-coding regions in hypoxic-ischaemic regulated genes in different species Proceeding/Conference:50th Anniversary Symposium on Paediatric Neurology & Neuro-Rehabilitation	Fu, W Chung, BHY Smith, DK Cheung, PT	2005
	Automated method for the identification of conserved non-coding regions in hypoxic-ischaemic regulated genes in different species Proceeding/Conference:Hong Kong Medical Genetics Conference	Fu, W Chung, BHY Smith, DK Cheung, PT	2005
	Bioinformatic piepline for the identification of transcription factor binding sites in mouse and human Proceeding/Conference:HUGO / HUGO-AP 2006	Fu, W Chung, BHY Smith, DK Cheung, PT	2006
	Bioinformatic pipeline for the identification of transciption factor binding sites in mouse and human Proceeding/Conference:HUGO Annual Human Genome Meeting, HGM 2006	Fu, W Chung, BHY Smith, DK	2006
	Bioinformatic pipeline for the identification of transcription factor binding sites in mouse and human Proceeding/Conference:HKPS-HKPNA 2006 Joint Annual Scientific Meeting	Fu, W Chung, BHY Smith, DK Cheung, PT	2006
	A family with osteoporosis pseudoglioma syndrome due to compound heterozygosity of two novel mutations in the LRP5 gene Journal:Bone	Cheung, WMW Jin, LY Smith, DK Cheung, PT Kwan, EYW Low, L Kung, AWC	2006
	Family with osteoporosis Pseudolioma Syndrome due to compound heterozygosity of two novel mutations of the LRP5 gene Proceeding/Conference:Annual Scientific Meeting of the Osteoporosis Society of Hong Kong, OSHK 2005	Jin, L Lau, HL Smith, DK Lau, KS Cheung, PT Kwan, EYW Low, LCK Chan, VNY Kung, AWC	2005
	A family with osteoporosis-pseudoglioma syndrome (OPG) due to compound heterozygous mutation of the LRO5 gene Proceeding/Conference:Journal of Bone and Mineral Research	Jin, L Lau, HL Smith, DK Lau, KS Cheung, PT Kwan, EYW Low, LCK Kung, AWC	2004
	A family with osteoporosis-pseudoglioma syndrome (OPG) due to compound heterozygous mutation of the LRP5 gene Proceeding/Conference:Medical Research Conference, MRC 2005	Jin, L Lau, HL Smith, DK Lau, KS Cheung, PT Kwan, EYW Low, LCK Chan, VNY Kung, AWC	2005
	HaploShare: identification of extended haplotypes shared by cases and evaluation against controls Journal:Genome Biology (Online Edition)	Ying, D Sham, PC Smith, DK Zhang, L Lau, YL Yang, W	2015
	Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups Journal:Nature Communications	Wang, YF Zhang, Y Lin, Z ZHANG, H Wang, TY CAO, Y Morris, DL Sheng, Y Yin, X Zhong, SL Gu, X LEI, Y He, J Wu, Q SHEN, J Yang, J Lam, TH Lin, JH Mai, Z GUO, M Tang, Y Chen, Y Song, Q Ban, B Mok, CC Cui, Y Lu, L Shen, N Sham, PC Lau, CS Smith, DK Vyse, TJ Zhang, X Lau, YL Yang, W	2021
	Identification of novel FBN1 and TGFBR2 mutations in 65 probands with Marfan syndrome or Marfan-like phenotypes Journal:American Journal of Medical Genetics, Part A	Chung, BHY Lam, STS Tong, TMF Li, SYH Lun, KS Chan, DHC Fok, SFS Or, JSF Smith, DK Yang, W Lau, YL	2009
	Sequence analysis for putative transcription factor binding sites of a novel hypoxic-ischaemic regulated gene - HID-1 Proceeding/Conference:Hong Kong Medical Genetics Conference	Fu, W Chung, BHY Chan, KW Bhatia, I Smith, DK Cheung, PT	2005
	Sequence analysis for putative transcription factor binding sites of a novel hypoxic-ischaemic regulated gene - HID-1 Proceeding/Conference:HKPS-HKPNA 2006 Joint Annual Scientific Meeting	Fu, W Chung, BHY Chan, KW Bhatia, I Smith, DK Cheung, PT	2006
	Sequence analysis of putative promoter sequences of known and novel genes identified by hpoxic-ischaemic insult Proceeding/Conference:Research Postgraduate Symposium, RPS 2005	Fu, W Chung, BHY Chan, KW Bhatia, I Smith, DK Cheung, PT	2005

Showing results 1 to 15 of 15