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Showing results 13 to 27 of 27 < previous

	Title	Author(s)	Issue Date	Views
	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	195
	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	147
	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	68
	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	68
	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	175
	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	133
	Novel single nucleotide polymorphism (9678G→A) for linkage analysis of acute intermittent porphyria [2] Journal:Clinical Chemistry	Law, WK Choy, KW Lam, CW	1999	108
	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	61
	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	86
	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	161
	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	112
	Reduced CRYL1 expression in hepatocellular carcinoma confers cell growth advantages and correlates with adverse patient prognosis Journal:Journal of Pathology	Cheng, IK Ching, AK Chan, TC Chan, AW Wong, CK Choy, KW Man, K Lai, PB Wong, N	2010	184
	Resolving the genetic heterogeneity of prelingual hearing loss within one family: Performance comparison and application of two targeted next generation sequencing approaches. Journal:Journal of Human Genetics	Yu, L Zhou, X Jin, Z Cheng, J Shen, W Ji, F Liui, L Zhang, X Zhang, MQ Cao, Y Han, D Choy, KW Yuan, H	2014	53

Showing results 13 to 27 of 27 < previous