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Showing results 6 to 10 of 10 < previous

	Title	Author(s)	Issue Date	Views
	Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanism Journal:EBioMedicine	Lam, WY Tang, SM So, MT Yue, H HSU, SJ Chung, HY Nicholls, JM Yeung, F Lee, DCW Ngo, DN Nguyen, PAH Mitchison, HM Jenkins, D O'Callaghan, C Garcia-Barcelo, MM Lee, SL Sham, PC Lui, VCH Tam, PKH	2021	10
	Robust and rapid algorithms facilitate large-scale whole genome sequencing downstream analysis in an integrative framework Journal:Nucleic Acids Research	Li, M LI, J Li, J Pan, Z HSU, SJ Liu, D Zhan, X Wang, JJ Song, Y Sham, PC	2017	102
	Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing Journal:European Journal of Human Genetics	Tang, SM Zhuang, X Lam, WY Ngan, ESW HSU, SJ Yu, M So, MT Cherny, SS Ngo, ND Sham, PC Tam, PKH Garcia-Barcelo, MM	2018	80
	Whole exome sequencing analysis in biliary atresia: a follow-up study Proceeding/Conference:68th Annual Meeting of the American Society of Human Genetics, 2018	Lam, WY Hsu, SJ Tang, SM So, MT Chung, HY Tam, PKH Garcia-Barcelo, MM	2018	51
	Whole exome sequencing reveals a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia Proceeding/Conference:The 67th Annual Congress of the British Association of Paediatric Surgeons (Virtual), U.K. 7-9 July 2022	Lam, WY So, MT HSU, SJ Chung, HY Ngo, DM Nguyen, PAH Mitchison, HM Jenkins, D O'Callaghan, C Sham, PC Garcia-Barcelo, MM Lui, VCH Tang, SM Tam, PKH	2021	11

Showing results 6 to 10 of 10 < previous