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TypeTitleAuthor(s)YearViews
Emphysematous pyelonephritis: an 8-year retrospective review across four acute hospitalsTsu, HLJ; Chan, CK; Chu, RWH; Law, IC; Kong, CK; Liu, PL; Cheung, FK; Yiu, MK201333
 
Emphysematous pyelonephritis: an eight-year retrospective review across four hospitals in a single clusterChan, CK; Tsu, JHL; Chu, WH; Kong, CK; Law, IC; Liu, PL; Yiu, MK2011152
 
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1Ligtenberg, MJL; Kuiper, RP; Chan, TL; Goossens, M; Hebeda, KM; Voorendt, M; Lee, TYH; Bodmer, D; Hoenselaar, E; HendriksCornelissen, SJB; Tsui, WY; Kong, CK; Brunner, HG; Van Kessel, AG; Yuen, ST; Van Krieken, JHJM; Leung, SY; Hoogerbrugge, N2009105
 
Deletion of the 3’ Exons of TACSTD1 Causes Hereditary Nonpolyposis Colorectal Cancer with MSH2 Gene Promoter MethylationChan, TL; Yuen, ST; Kuiper, RP; Lee, TYH; Tsui, WY; Lau, JKY; Li, C; Chan, KW; Kong, CK; Chan, ASY; Ligtenberg, MJL; Leung, SY2009247
 
Prospective randomized study of selective neck dissection versus observation for N0 neck of early tongue carcinomaYuen, PW; Ho, CM; Chow, TL; Tang, LC; Cheung, WY; Ng, WM; Wei, WI; Kong, CK; Book, KS; Yuen, WC; Lam, AK; Yuen, NW; Trendell-Smith, NJ; Chan, YW; Wong, BYH; Li, GKH; Ho, ACW; Ho, WK; Wong, SY; Yao, TJ2009392
 
Study of the mechanisms underlying heritable germline epimutation of MSH2 in a Hereditary Nonpolyposis Colorectal Cancer familyChan, TL; Yuen, ST; Lo, MWS; Lee, TYH; Kong, CK; Chan, YW; Tsui, WY; Li, VSW; Chan, ASY; Leung, SY2007190
 
Heritable germline epimutation of MSH2 in a hereditary nonpolyposis colorectal cancer familyChan, TL; Yuen, ST; Kong, CK; Chan, YW; Chan, ASY; Leung, SY2007202
 
Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancerChan, TL; Yuen, ST; Kong, CK; Chan, YW; Chan, ASY; Ng, WF; Tsui, WY; Lo, MWS; Tam, WY; Li, VSW; Leung, SY2006143
 
Atypical presentation of dopa-responsive dystonia: Generalized hypotonia and proximal weaknessKong, CK; Ko, CH; Tong, SF; Lam, CW2001108
 
De novo mutation in the mitochondrial tRNALeu(UUR) gene (A3243G) with rapid segregation resulting in MELAS in the offspringKo, Ch; Lam, CW; Tse, PWT; Kong, CK; Chan, AKH; Wong, LJC200188
 
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