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Showing results 1 to 5 of 5

	Title	Author(s)	Issue Date
	A three-year follow up study on 104 exome-sequenced patients with paediatric-onset diseases: Exome reanalysis and the impacts on clinical management and outcome Proceeding/Conference:European Human Genetics Virtual Conference: ESHG 2020.2 - Live in your Living Room, 2020	Fung, LF Huang, S Yu, HC Chung, CY Chan, MCY Pajusalu, S Lek, M Chung, BHY	2020
	A three-year follow-up study evaluating clinical utility of exome sequencing and diagnostic potential of reanalysis Journal:npj Genomic Medicine	Fung, JLF YU, MHC Huang, S CHUNG, CCY Chan, MCY Pajusalu, S Mak, CCY Hui, VCC TSANG, MHY Yeung, KS Lek, M Chung, BHY	2020
	Exome sequencing in paediatric patients with movement disorders [accepted - OJRD-D-20-00713R2] Journal:Orphanet Journal of Rare Diseases	Kwong, AKY TSANG, MHY Fung, JLF Mak, CCY Chan, KLS Rodenburg, RJT Lek, M Huang, S Pajusalu, S Yau, MM Tsoi, C Fung, S Liu, KT Ma, CK Wong, S Yau, EKC Tai, SM Fung, ELW Wu, NSP Tsung, LY Smeitink, J Chung, BHY Fung, CW	2021
	Reanalyzing clinical whole exome sequencing (WES) data aprovides additional diagnosis in paediatric-onset undiagnosed diseases – a Yale-HKU collaborative study 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	Fung, LF Huang, S Pajusalu, S Yu, HC Chan, M Mak, C Hui, V Chung, CY Lek, M Chung, BHY	2019
	Reanalyzing clinical whole exome sequencing (WES) data provides additional diagnosis in paediatric-onset undiagnowed diseases – A Yale-HKU collaboration Proceeding/Conference:Asia-Pacific Conference on Human Genetics (APCHG) 2019	Fung, LF Huang, S Pajusalu, S YU, HC Chan, M Lek, M Chung, BHY	2019

Showing results 1 to 5 of 5