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Showing results 1 to 11 of 11

	Title	Author(s)	Issue Date
	Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies—Experience from a Local Prenatal Diagnostic Laboratory Journal:Healthcare	Lai, HTT Lau, ETK Lau, YTE Lo, HM Chan, YK Cheung, KW Ma, TWL Leung, WC Kong, CW Shu, W So, PL Kwong, KY Mak, CCY Lee, M Chui, MCM Chung, BHY Kan, SYA	2022
	Automatic parallelization and scheduling of programs on multiprocessor using CASCH Proceeding/Conference:International Conference on Parallel Processing Proceedings	Ahmad, I Kwok, YK Wu, MY Shu, W	1997
	CASCH: a tool for computer-aided scheduling Journal:IEEE Concurrency	Ahmad, I Kwok, YK Wu, MY Shu, W	2000
	Deguelin represses both the expression of nucleophosmin and some nucleoporins: Nup88 and Nup214 in Jurkat cells Journal:Biological and Pharmaceutical Bulletin	Shu, W Chen, Y Wu, Q Li, R Cui, G	2008
	Effect of Gambogic acid on the regulation of hERG channel in K562 cells in vitro Journal:Journal of Huazhong University of Science and Technology - Medical Science	Cui, G Shu, W Wu, Q Chen, Y	2009
	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
	A Graphical Tool for Automatic Parallelization and Scheduling of Programs on Multiprocessors Proceeding/Conference:Proceedings of the 3rd European Conference on Parallel Processing (EURO-PAR'97) (LNCS 1300)	Kwok, YK Ahmad, I Wu, MY Shu, W	1997
	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
	Let the History Have a Less Regret: A discussion on preservation and development of historical town Lijiang Book:Architect	Jia, B Yang, D Lu, Q Xu, Y Pan, A Shu, W Lu, Y Dai, Z Yu, Y Yan, Y Guo, Z	1998
	Prenatal diagnosis and ultrasound features of Harlequin Ichthyosis Proceeding/Conference:Ultrasound in Obstetrics and Gynecology	Hui, PW Seto, TYM Shu, W Lee, C	2018
	Prenatal presentation in two fetuses with features of Beckwith Wiedemann syndrome—An unexpected diagnosis of androgenetic chimera and its clinical implications Journal:American Journal of Medical Genetics Part A	Yu, PT Shu, W Mok, SL Hui, PW Chan, LW Kwok, KY Chan, YK Lo, TK Chung, BHY Luk, HM Kan, SYA	2022

Showing results 1 to 11 of 11