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Showing results 1 to 10 of 10

	Title	Author(s)	Issue Date
	A dominant negative mutation at the ATP binding domain of AMHR2 is associated with a defective anti-Müllerian hormone signaling pathway Journal:Molecular Human Reproduction	Li, L Zhou, X Wang, X Wang, J Zhang, W Wang, B Cao, Y Kee, K	2016
	A Practical Guide for Mapping Short Reads Book:Deep Sequencing Data Analysis	Zhou, X Bao, S Wang, B Zhang, X Song, Y	2013
	A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese population Journal:Neurobiology of Aging	Wang, B Bao, S ZHANG, Z ZHOU, X WANG, J Fan, Y Zhang, Y Li, Y Chen, LP Jia, Y LI, J Li, M Zheng, W Mu, N Yang, W Yu, Z Lau, DSS Wong, SM ZHANG, Y Kwan, JSK Mak, HKF Ambalavanan, A Zhou, S Cai, W Zheng, J Huang, S Rouleau, GA Yang, W Rogaeva, E Ma, X St George-Hyslop, P Chu, LW Song, Y	2018
	CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens Journal:Scientific Reports	Wang, B Ji, T Zhou, X Wang, J Wang, X Wang, JM Zhu, D Zhang, XJ Sham, PC Zhang, XG Ma, X Jiang, Y	2016
	Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases Journal:Nucleic Acids Research	Jiang, L Jiang, H Dai, S Chen, Y Song, Y Tang, SM Pang, SYY Ho, SL Wang, B Garcia-Barcelo, MM Tam, PKH Cherny, SS Li, MJ Sham, PC Li, M	2022
	Exome Sequencing and Gene Prioritization Correct Misdiagnosis in a Chinese Kindred with Familial Amyloid Polyneuropathy Journal:Scientific Reports	Chen, H Zhou, X Wang, J Wang, X Liu, L Wu, S Li, T Chen, S Yang, J Sham, PC Zhu, G Zhang, X Wang, B	2016
	Hnrnpa1 Mutations Cause Congenital Heart Defects Proceeding/Conference:Hong Kong Inter-University Postgraduate Symposium in Biochemical Sciences, 2017	Yu, Z Tang, PLF Wang, J Bao, S Shieh, JT Leung, AWL Zhang, Z Gao, F Wong, SYY Hui, ALC Gao, Y Dung, NWF Zhang, ZG Fan, Y Zhou, X Zhang, Y Wong, DSM Sham, PC Azhar, A Kwok, PY Tam, PPL Lian, Q Cheah, KSE Wang, B Song, Y	2017
	Mapping of a Hirschsprung's disease locus in 3p21 Journal:European Journal of Human Genetics	GarciaBarceló, MM Fong, PY Tang, CS Miao, XP So, MT Yuan, ZW Li, L Guo, WH Liu, L Wang, B Sun, XB Huang, LM Tou, JF Wong, KKY Ngan, ESW Lui, VCH Cherny, SS Sham, PC Tam, PKH	2008
	Mutational analysis of SHH and GLI3 in anorectal malformations Journal:Birth Defects Research Part A - Clinical and Molecular Teratology	GarciaBarceló, MM Lui, VCH Miao, X So, MT Leon, TYY Yuan, ZW Li, L Liu, L Wang, B Sun, XB Huang, LM Tou, JF Ngan, ESW Cherny, SS Chan, KW Lee, KH Wang, W Wong, KKY Tam, PKH	2008
	RET mutational spectrum in Hirschsprung disease: Evaluation of 601 Chinese patients Journal:PLoS ONE	So, MT LeonThomas, YY Cheng, G TangClara, SM Miao, XP Cornes, BK Ngo, DN Cui, L NganElly, SW LuiVincent, CH Wu, XZ Wang, B Wang, H Yuan, ZW Huang, LM Li, L Xia, H Zhu, D Liu, J Nguyen, TL ChanIvy, HY Chung, HY Liu, XL Zhang, R Wong, KKY Sham, PC Cherny, SS Tam, PKH GarciaBarcelo, MM	2011

Showing results 1 to 10 of 10