| Title | Author(s) | Year | View Count |
 | A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13 | Zaidi, SHE; Peltekova, V; Meyer, S; Lindinger, A; Paterson, AD; Tsui, LC; FaiyazUlHaque, M; Teebi, AS | 2005 | 548 |
| Fat embolism in Hong Kong Chinese | Chow, SP; Hoaglund, FT | 1980 | 33 |
 | Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1 | Scherer, SW; Poorkaj, P; Allen, T; Kim, J; Geshuri, D; Nunes, M; Soder, S; Stephens, K; Pagon, RA; Patton, MA; Berg, MA; Donlon, T; Rivera, H; Pfeiffer, RA; Naritomi, K; Hughes, H; Genuardi, M; Gurrieri, F; Neri, G; Lovrein, E; Magenis, E; Tsui, L-C; Evans, JP | 1994 | 264 |
 | Fine mapping of the human and mouse genes for the type i procollagen COOH-terminal proteinase enhancer protein | Takahara, K; Osborne, L; Elliott, RW; Tsui, LC; Scherer, SW; Greenspan, DS | 1996 | 236 |
| Fine mapping of the X-linked split-hand/split-foot malformation (SHFM2) locus to a 5.1-Mb region on Xq26.3 and analysis of candidate genes | FaiyazUlHaque, M; Zaidi, SHE; King, LM; Haque, S; Patel, M; Ahmad, M; Siddique, T; Ahmad, W; Tsui, LC; Cohn, DH | 2005 | 857 |
| FISH detection on DAPI-banded chromosomes. | Heng, HH; Tsui, LC | 1994 | 78 |
| Fluorescence in situ hybridization mapping of the cystic fibrosis transmembrane conductance regulator (CFTR) gene to 7q31.3 | Heng, HHQ; Shi, XM; Tsui, LC | 1993 | 287 |
| Fluorescent in situ mapping of the murine deleted in split hand/split foot 1 (dss1) gene to Chromosome 6 | Crackower, MA; Heng, HHQ; Shi, X; Scherer, SW; Tsui, LC | 1997 | 97 |
| Fracture of the tibial tubercle in the adolescent | Chow, SP; Lam, JJ; Leong, JCY | 1990 | 30 |
| Frameshift mutation in the cartilage-derived morphogenetic protein 1 (CDMP1) gene and severe acromesomelic chondrodysplasia resembling Grebe-type chondrodysplasia | FaiyazUlHaque, M; Ahmad, W; Wahab, A; Haque, S; Azim, AC; Zaidi, SHE; Teebi, AS; Ahmad, M; Cohn, DH; Siddique, T; Tsui, LC | 2002 | 259 |
| A frameshift mutation in the γE-crystallin gene of the Elo mouse | Cartier, M; Breitman, ML; Tsui, LC | 1992 | 210 |
| Free chromatin mapping by FISH. | Heng, HH; Tsui, LC | 1994 | 71 |
| Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiency | Lu, YB; Kobayashi, K; Ushikai, M; Tabata, A; Iijima, M; Li, MX; Lei, L; Kawabe, K; Taura, S; Yang, Y; Liu, TT; Chiang, SH; Hsiao, KJ; Lau, YL; Tsui, LC; Lee, DH; Saheki, T | 2005 | 789 |
| From "Brain Drain" to "Brain Circulation" - rethinking the global knowledge economy: perspective from Hong Kong | Tam, Paul KH | 2009 | 162 |
| Further data on linkage between cystic fibrosis and 7C22 (D7S16) | Farrall, M; Lathrop, M; Spence, JE; Bowcock, A; Klinger, K; Tsui, LC | 1987 | 196 |
| Gamma-crystallins of the human eye lens: expression analysis of five members of the gene family. | Meakin, SO; Du, RP; Tsui, LC; Breitman, ML | 1987 | 321 |
| Gene Mapping By Hybridization To Free Chromatin | Heng, HHQ; Tsui, L-C | - | 513 |
| The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein | Kobayashi, K; Sinasac, DS; Iijima, M; Boright, AP; Begum, L; Lee, JR; Yasuda, T; Ikeda, S; Hirano, R; Terazono, H; Crackower, MA; Kondo, I; Tsui, LC; Scherer, SW; Saheki, T | 1999 | 292 |
| Gene structure and chromosome localization to 7q21.3 of the human rod photoreceptor transducin γ-subunit gene (GNGT1) | Scherer, SW; Feinstein, DS; Oliveira, L; Tsui, LC; Pittler, SJ | 1996 | 235 |
| Gene structure of the human MET proto-oncogene | Duh, FM; Scherer, SW; Tsui, LC; Lerman, MI; Zbar, B; Schmidt, L | 1997 | 425 |
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