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Showing results 169 to 181 of 181 < previous

	Title	Author(s)	Issue Date
	Targeting granulin-epithelin precursor in breast cancer Proceeding/Conference:Cancer Research	Ip, YC Chan, YK Wong, ASY Cheung, ST Khoo, US	2009
	The forkhead transcription factor FOXO3a increases Akt activity in breast cancer cell lines through a feed-back mechanism. Proceeding/Conference:Hong Kong International Cancer Congress, HKICC 2011	Chen, J Chan, YK Wu, LH Ip, YC Lam, EW Khoo, US	2011
	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
	The KLHL40C.1516A>C is a Chinese-specific founder mutation in causing nemaline myopathy 8 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	Yeung, KS Yu, YN Fung, CW Wong, S Lee, HCH Fung, STH Fung, GPG Yu, MHC Fung, JLF Tsang, MHY Chan, YK Chan, HSS Kan, SYA Chung, BHY	2019
	The tandem repeat polymorphism of the DC-SIGNR gene is associated with susceptibility to SARS coronavirus infection in Chinese from Hong Kong Proceeding/Conference:HUGO annual Human Genome Meeting, HGM 2004	Khoo, US Chan, KYK Yip, VSP Peiris, JSM Tin, V Liu, W Xue, W Ngan, HYS Chan, LC Cheung, ANY	2004
	Two IUGR foetuses with maternal uniparental disomy of chromosome 6 or UPD(6)mat Journal:Journal of Obstetrics and Gynaecology	Leung, WC Lau, WL Lo, TK Lau, TK Lam, YY Kan, SYA Chan, YK Lau, ETK Tang, MHY	2017
	Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: Implications in transitional care Journal:European Journal of Medical Genetics	Liu, APY Chow, PC Lee, PPW Mok, GTK Tang, WF Lau, ETK Lam, STS Chan, YK Kan, SYA Chau, AKT Cheung, YF Lau, YL Chung, BHY	2014
	Use of chromosomal microarray in Hong Kong patients with autism spectrum disorder - implication of a copy number variation involving DPP10 Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2016	Chung, BHY Mak, SL Chiu, TA Leung, KC Mak, CCY Chu, WY Mok, TKG Chan, YK Kan, SYA Tang, MHY Lau, ETK Fung, CW Lee, SL	2016
	Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving DPP10 Journal:Molecular Autism	Mak, ASL Chiu, TA Leung, KC Mak, CCY Chu, WY Mok, TKG Tang, WF Chan, YK Tang, MHY Lau, ETK So, KW Tao, QV Fung, CW Wong, CNV Uddin, M Lee, SL Marshall, CR Scherer, SW Kan, ASY Chung, BHY	2017
	Use of clinical chromosomal microarray in Hong Kong Chinese patients with autism spectrum disorder - implication of a copy number variation involving DPP10 Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Chu, YWY Leung, KC Mak, ASL Chiu, TA Mak, CCY Mok, TKG Tang, WF Chan, YK Tang, MHY Lau, ETK So, KW Tao, QV Fung, CW Wong, VCN Lee, SL Marshall, C Scherer, S Kan, SYA Chung, BHY	2016
	A variant in the CD209 promoter is associated with severity of Severe Acute Respiratory Syndrome (SARS) Proceeding/Conference:HUGO Annual Human Genome Meeting, HGM 2006	Xu, MS Chan, YK Peiris, JSM Yip, SP Cheung, ANY Khoo, US	2006
	Whole-Genome Array CGH Evaluation for Replacing Prenatal Karyotyping in Hong Kong Journal:PLoS ONE	Kan, SYA Lau, ETK Tang, WF Chan, SSY Ding, SCK Chan, YK Lee, CP Hui, PW Chung, BHY Leung, KY Ma, WLT Leung, WC Tang, MHY	2014
	Women’s stated test preference on questionnaire versus their actual choice in real clinical setting regarding non-invasive prenatal test Journal:European Journal of Obstetrics & Gynecology and Reproductive Biology	Lo, TK Chan, YK Kan, SYA So, PL Kong, CW Mak, SL Lee, CN	2017

Showing results 169 to 181 of 181 < previous