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Results 2424 to 2443 of 5772
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TypeTitleAuthor(s)YearViews
'I don’t want to see my children suffering after birth': The ‘risk of knowing’ talk and decision-making in prenatal screening for Down syndrome in Hong KongYAU, HYA; Zayts, OA201330
 
I grew mushroomsLam, ASL200498
 
I grew mushroomsLam, ASL2008101
 
I have walked on airLam, ASL2003103
 
"I wish to be self-reliant": Aspiration for self-reliance, need and life satisfaction, and exit dilemma of welfare recipients in Hong KongWong, CK; Lou, VWQ2010262
 
I wish to be self-reliant: aspiration for self-reliance, need and life satisfaction, and exit dilemma of welfare recipients in Hong KongWong, CK; Lou, VW2011170
 
An ice-skating program for the children with mental disabilitiesHo, WO; Sit, HP200672
 
IClass assessment: a pen-based assessment and feedback platformFok, WWT; Chan, CKY201328
 
ICT implementation and school leadership: Case studies of ICT integration in teaching and learningYuen, HK; Law, NWY; Wong, KC2003833
 
Identification and characterization of human genes encoding Hprp3p and Hprp4p, interacting components of the spliceosomeWang, A; FormanKay, J; Luo, Y; Luo, M; Chow, YH; Plumb, J; Friesen, JD; Tsui, LC; Heng, HHQ; Woolford Jr, JL; Hu, J1997374
 
Identification and characterization of proteins interacting with SIRT1 and SIRT3: implications in the antiaging and metabolic effects of sirtuinsLaw, IKM; Liu, L; Xu, A; Lam, KSL; Vanhoutte, PM; Che, CM; Leung, PTY; Wang, Y2009125
 
The identification and development of essential attributes for expert sports performance.Abernethy, AB200774
 
Identification and functional expression of HCx31.9, a novel gap junction geneBelluardo, N; White, TW; Srinivas, M; TrovatoSalinaro, A; Ripps, H; Mudò, G; Bruzzone, R; Condorelli, DF2001100
 
Identification and regional localization of DNA markers on chromosome 7 for the cloning of the cystic fibrosis geneRommens, JM; Zengerling, S; Burns, J; Melmer, G; Kerem, B; Plavsic, N; Zsiga, M; Kennedy, D; Markiewicz, D; Rozmahel, R; Riordan, JR; Buchwald, M; Tsui, L1988287
 
Identification of a 1300 kilobase deletion unit on chromosome 7q31.3 in invasive epithelial ovarian carcinomasEdelson, MI; Scherer, SW; Tsui, LC; Welch, WR; Bell, DA; Berkowitz, RS; Mok, SC1997111
 
Identification of a human LIM-Hox gene, hLH-2, aberrantly expressed in chronic myelogenous leukaemia and located on 9q33-34.1Wu, HK; Heng, HHQ; Siderovski, DP; Dong, WF; Okuno, Y; Shi, XM; Tsui, LC; Minden, MD1996118
 
Identification of a novel lipase gene mutated in lpd mice with hypertriglyceridemia and associated with dyslipidemia in humansWen, XY; Hegele, RA; Wang, J; Yan Wang, D; Cheung, J; Wilson, M; Yahyapour, M; Bai, Y; Zhuang, L; Skaug, J; Young, TK; Connelly, PW; Koop, BF; Tsui, LC; Stewart, AK2003710
 
Identification of a p.Ser81Arg encoding mutation in SLC2A10 gene of arterial tortuosity syndrome patients from 10 Qatari familiesFaiyazulHaque, M; Zaidi, SHE; Wahab, AA; Eltohami, A; AlMureikhi, MS; AlThani, G; Peltekova, VD; Tsui, LC; Teebi, AS2008136
 
Identification of a polymorphic DNA marker pDL32B (D12S7) and its localization to the long arm of chromosome 12, region q14.3-qterTsui, LC; Buchwald, M; Markiewicz, D; Kao, FT; Cai, GY; Law, ML1985288
 
Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndromeOsborne, LR; Campbell, T; Daradich, A; Scherer, SW; Tsui, LC1999184
 
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