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Showing results 1 to 14 of 14

	Title	Author(s)	Issue Date
	Clinical Characteristics and gp91phox Gene Mutations in Seventeen Chinese Children with X-linked Chronic Granulomatous Disease Proceeding/Conference:Congress of Asian Society for Pediatric Research, ASPR 2006	Lee, PPW Chan, KW Lee, TL Jiang, L Mak, HS Fok, SFS Hui, YF Li, C Yang, X Lau, YL	2006
	Correspondence: further studies on a kindred reported by Li 2009 as ‘A new syndrome of ankyloglossia and ulnar ray defects in Newfoundland kindred’. From ‘new syndrome’ through EEC to ulnar mammary syndrome (Letter to the Editor) Journal:Clinical Dysmorphology	Chung, BHY Fernandez, B Li, C Chitayat, D	2012
	De novo C-terminal truncating mutations in MN1 cause a neurodevelopmental syndrome with distinctive facial features Proceeding/Conference:European Human Genetics Conference, 2019	Gordon, CT Leung, KC Mak, CCY Doherty, D Lin, A Vegas, N Cho, M Dimartino, C Weisfeld-Adams, J Lessel, D Joss, S Li, C Gonzaga-Jauregui, C Zarate, Y Troyer, C Kant, S Leung, G Barone, A Yang, S Bend, E Roadhouse, C Zahir, F Stolerman, E Bienvenu, T Orenstein, N Dobyns, W Shieh, J Waggoner, D Gripp, K Parker, M Stoler, J Lyonnet, S Cormiere-Daire, V Viskochil, D Hoffman, T Amiel, J Chung, BHY	2019
	Human cytomegalovirus matrix protein PP150 is efficiently presented as one of target antigens for cytotoxic T lymphocyte recognition Journal:Chinese Medical Journal	Li, C Yang, X Tu, W Riddell, SR	1997
	Insult of immune functions in children of subclinical vitamin A deficiency: an investigative report of 80 cases Journal:Clinical Journal of Pediatrics	Li, W Yang, X Li, C Tu, W	1997
	Mental Health of Children With Special Educational Needs and the Return to In-Person Learning After the COVID-19 Pandemic Journal:Jama Network Open	Tso, WWY Leung, LK Chow, MSC Wang, Y Li, C Hui, KY Ma, L Wong, MW Lui, MPK Wong, WHS Lee, SL Lee, TMC Ip, P	7-Dec-2023
	Meta-analysis of 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus Journal:Annals of the Rheumatic Diseases	Yin, X Kim, K Suetsugu, H Bang, SY Wen, L Koido, M Ha, E Liu, L Sakamoto, Y Jo, S Leng, RX Otomo, N Laurynenka, V Kwon, YC Sheng, Y Sugano, N Hwang, MY Li, W Mukai, M Yoon, K Cai, M Ishigaki, K Chung, WT Huang, H Takahashi, D Lee, SS Wang, M Karino, K Shim, SC Zheng, X Miyamura, T Kang, YM Ye, D Nakamura, J Suh, CH Tang, Y Motomura, G Park, YB Ding, H Kuroda, T Choe, JY Li, C Niiro, H Park, Y Shen, C Miyamoto, T Ahn, GY Fei, W Takeuchi, T Shin, JM Li, K Kawaguchi, Y Lee, YK Wang, Y Amano, K Park, DJ Yang, W Tada, Y Yamaji, K Shimizu, M Atsumi, T Suzuki, A Sumida, T Okada, Y Matsuda, K Matsuo, K Kochi, Y Kottyan, LC Weirauch, MT Parameswaran, S Eswar, S Salim, H Chen, X Yamamoto, K Harley, JB Ohmura, K Kim, TH Yang, S Yamamoto, T Kim, BJ Shen, N Ikegawa, S Lee, HS Zhang, X Terao, C Cui, Y Bae, SC	2020
	MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis Journal:Brain	Mak, CCY Doherty, D Lin, AE Vegas, N Cho, MT Viot, G Dimartino, C Weisfeld-Adams, JD Lessel, D Joss, S Li, C Gonzaga-Jauregui, C Zarate, YA Ehmke, N Horn, D Troyer, C Kant, SG Lee, Y Ishak, GE Leung, G Barone Pritchard, A Yang, S Bend, EG Filippini, F Roadhouse, C Lebrun, N Mehaffey, MG Martin, P-M Apple, B Millan, F Puk, O Hoffer, MJV Henderson, LB McGowan, R Wentzensen, IM Pei, S Zahir, FR YU, M Gibson, WT Senab, A Steeves, M Murrell, JR Luettgen, S Francisco, E Strom, TM Amlie-Wolf, L Kaindl, AM Wilson, WG Halbach, S Basel-Salmon, L Lev-El, N Denecke, J Vissers, LELM Radtke, K Chelly, J Zackai, E Friedman, JM Bamshad, MJ Nickerson, DA Reid, RR Devriendt, K Chae, JH Stolerman, E McDougall, C Powis, Z Bienvenu, T Tan, TY Orenstein, N Dobyns, WB Shieh, JT Choi, M Waggoner, D Gripp, KW Parker, MJ Stoler, J Lyonnet, S Cormier-Daire, V Viskochil, D Hoffman, TL Amiel, J Chung, BHY Gordon, CT University of Washington Center for Mendelian Genomics	2020
	Population-based treatment results of hepatoblastoma in children of Hong Kong Proceeding/Conference:Pediatric Blood & Cancer	Chiang, AK Ling, SC Li, C Yuen, H Cheuk, DKL Li, CB	2013
	Severe intellectual disability and autistic features associated with microduplication 2q23.1 Journal:European Journal of Human Genetics	Chung, BHY Mullegama, S Marshall, CR Lionel, AC Weksberg, R Dupuis, L Brick, L Li, C Scherer, SW Aradhya, S Stavropoulos, DJ Elsea, SH MendozaLondono, R	2012
	Susceptibility to mycobacterial infections in children with x-linked chronic granulomatous disease: A review of 17 patients living in a region endemic for tuberculosis Journal:Pediatric Infectious Disease Journal	Lee, PPW Chan, KW Jiang, L Chen, T Li, C Lee, TL Mak, PHS Fok, SFS Yang, X Lau, YL	2008
	Treatment barriers and clinical outcome of children with medulloblastoma in China: a report from the Chinese Children’s Cancer Group (CCCG) Journal:Neuro-Oncology Advances	Liu, APY Zhen, Z Yang, Q Yuan, X Ma, X Chen, J Wang, J Yang, L Guo, H Jiang, L Weng, W Huang, L Liu, W Wang, J Wu, S Zeng, J Jiang, M He, K Ge, M Cheng, KKF Ho, WWS Li, C Yu, L Zhu, S Ng, HK Chan, GCF Sun, X	2021
	Ulnar-Mammary Syndrome: expending the phenotype to include ankyloglossia and cleft lip and palate Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2010	Jessen, J Chung, BHY Fernandez, B Li, C Chitayat, D	2010
	Virus evasion of the immune system: cytokines, oncogenes, and apoptosis Proceeding/Conference:Symposium in Medical Sciences, 21st Century Health Care in Hong Kong: A New Era	Lau, ASY Lee, DCW Cheung, BKW Li, C	2002

Showing results 1 to 14 of 14