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Title	Author(s)	Issue Date	Views
Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice Journal:Journal of Medical Genetics	Bruno, DL Ganesamoorthy, D Schoumans, J Bankier, A Coman, D Delatycki, M Gardner, RJM Hunter, M James, PA Kannu, P Mcgillivray, G Pachter, N Peters, H Rieubland, C Savarirayan, R Scheffer, IE Sheffield, L Tan, T White, SM Yeung, A Bowman, Z Ngo, C Choy, KW Cacheux, V Wong, L Amor, DJ Slater, HR	2009	64
Determination of ofloxacin and moxifloxacin and their penetration in human aqueous and vitreous humor by using high-performance liquid chromatography fluorescence detection Journal:Analytical Biochemistry	Chan, KP Chu, KO Lai, WWK Choy, KW Wang, CC Lam, DSC Pang, CP	2006	84
Differential Aqueous and Vitreous Concentrations of Moxifloxacin and Ofloxacin After Topical Administration One Hour before Vitrectomy Journal:American Journal of Ophthalmology	Lai, WW Chu, KO Chan, KP Choy, KW Wang, CC Tsang, CW Pang, CP	2007	71
Establishment and characterization of a novel primary hepatocellular carcinoma cell line with metastatic ability in vivo Journal:Cancer Cell International	Cheung, PFY Yip, CW Ng, WCL Lo, KW Wong, N Choy, KW Chow, C Chan, KF Cheung, TT Poon, RTP Fan, ST Cheung, ST	2014
Exome Sequencing Identifies a Novel Frameshift Mutation of MYO6 as the Cause of Autosomal Dominant Nonsyndromic Hearing Loss in a Chinese Family Journal:Annals of Human Genetics	Cheng, J Zhou, X Lu, Y Chen, J Han, B Zhu, Y Liu, Y Choy, KW Sham, PC Zhang, MQ Zhang, X Yuan, H Yuan, H	2014
First Case Report of Maternal Mosaic Tetrasomy 9p Incidentally Detected on Non-Invasive Prenatal Testing Journal:Genes	Shu, W Cheng, SS.W.Xue, S Chan, LW Soong, SI Kan, SYA Cheung, SWH Choy, KW	2021	4
Glucose-6-phosphatase gene (727G→T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type 1a Journal:Clinical Genetics	Lam, CW But, WM Shek, CC Tong, SF Chan, YS Choy, KW Tse, WY Pang, CP Hjelm, NM	1998
Identification of a novel 12p13.3 amplicon in nasopharyngeal carcinoma Journal:Journal of Pathology	Or, YYY Chung, GTY To, KF Chow, C Choy, KW Tong, CYK Leung, AWC Hui, ABY Tsao, SW Ng, HK Yip, TTC Busson, P Lo, KW	2010	207
Implementation of Public Funded Genome Sequencing in Evaluation of Fetal Structural Anomalies Journal:Genes	So, PL Hui, AST Ma, TWL Shu, W Hui, PW Kong, CW Lo, TK Kan, ABC Kan, EYL Chong, SC Chung, BHY Luk, HM Choy, KW Kan, SYA Leung, WC	2022
Inhibition of NOTCH3 signalling significantly enhances sensitivity to cisplatin in EBV-associated nasopharyngeal carcinoma Journal:Journal of Pathology	Man, CH Lun, SWM Hui, JWY To, KF Choy, KW Chan, AWH Chow, C Chung, GTY Tsao, SW Yip, TTC Busson, P Lo, KW	2012	167
MicroRNA-19a-PTEN Axis Is Involved in the Developmental Decline of Axon Regenerative Capacity in Retinal Ganglion Cells Journal:Molecular Therapy - Nucleic Acids	Leung, KS Mak, HK Yung, SYJ Ho, YCT Ng, SH Cao, X Ng, TK Chu, WK Yung, WH Choy, KW Weinreb, RN Wang, CC Lee, TL	2021
miR-31 is consistently inactivated in EBV-associated nasopharyngeal carcinoma and contributes to its tumorigenesis Journal:Molecular Cancer	Cheung, CCM Chung, GTY Lun, SWM To, KF Choy, KW Lau, KM Siu, SPK Guan, X Ngan, RKC Yip, TTC Busson, P Tsao, GSW Lo, KW	2014
Monozygotic dichorionic twins heterokaryotypic for duplication chromosome 2q13-q23.3 Journal:Fetal Diagnosis and Therapy	Leung, WC Choi, H Lau, WL Ng, LK Lau, ET Lo, FM Choy, KW Lau, TK Tang, MHY Chin, R	2009	85
Mutation of proline 409 to arginine in the meander region of cytochrome P450c17 causes severe 17α-hydroxylase deficiency Journal:Molecular Genetics and Metabolism	Lam, CW Arlt, W Chan, CK Honour, JW Lin, CJ Tong, SF Choy, KW Miller, WL	2001	185
Novel and homozygous best1 mutations in chinese patients with best vitelliform macular dystrophy Journal:Retina	Wong, RLM Hou, P Choy, KW Chiang, SWY Tam, POS Li, H Chan, WM Lam, DSC Pang, CP Lai, TYY	2010	143
Novel single nucleotide polymorphism (9678G→A) for linkage analysis of acute intermittent porphyria [2] Journal:Clinical Chemistry	Law, WK Choy, KW Lam, CW	1999	115
Paeonol Attenuates LPS-Induced Endothelial Dysfunction and Apoptosis by Inhibiting BMP4 and TLR4 Signaling Simultaneously but Independently Journal:The Journal of Pharmacology and Experimental Therapeutics	Choy, KW Lau, YS Murugan, D Vanhoutte, PMGR Mustafa, MR	2018	71
Prenatal findings and delineation of de novo concurrent partial trisomy 7q(7q31.2 → qter) and partial monosomy 6q(6q26 → qter) by high-resolution array CGH Journal:Journal of Maternal-Fetal and Neonatal Medicine	Choy, KW Chan, LW Tang, MHY Ng, LKL Leung, TY Lau, TK	2009	96
Recurrent BRCA1 and BRCA2 germline mutations in ovarian cancer: a founder mutation of BRCA1 identified in the Chinese population. Journal:Human mutation	Khoo, US Chan, KY Cheung, AN Xue, WC Shen, DH Fung, KY Ngan, HY Choy, KW Pang, CP Poon, CS Poon, AY Ozcelik, H	2002	173
Recurrent BRCA2 mutation is found in Chinese ovarian cancer patients Proceeding/Conference:HKICC / RPS 2000	Fung, KY Chan, YK Poon, AYA Cheung, ANY Ngan, HYS Choy, KW Pang, CP Poon, CSP Khoo, US	2000

Showing results 6 to 25 of 27 < previous next >