| Title | Author(s) | Year | View Count |
 | Large-scale sequencing of two regions in human chromosome 7q22: Analysis of 650 kb of genomic sequence around the EPO and CUTL1 loci reveals 17 genes | Glockner, G; Scherer, S; Schattevoy, R; Boright, A; Weber, J; Tsui, LC; Rosenthal, A | 1998 | 226 |
 | Lens-specific promoter activity of a mouse g-crystallin gene | Lok, S; Breitman, ML; Chepelinsky, AB; Piatigorsky, J; Gold, RJM; Tsui, L-C | 1985 | 261 |
 | Linkage between the loci for cystic fibrosis and paraoxonase | Schmiegelow, K; Eiberg, H; Tsui, LC | 1986 | 301 |
| Linkage of cystic fibrosis to the proα2(I) collagen gene, COL1A2, on chromosome 7 | Buchwald, M; Zsiga, M; Markiewicz, D; Plavsic, N; Kennedy, D; Zengerling, S; Willard, HF; Tsipouras, P; Schmiegelow, K; Schwartz, M; Eiberg, H; Mohr, J; Barker, D; Donis-Keller, H; Tsui, LC | 1986 | 308 |
| Linkage of cystic fibrosis to two tightly linked DNA markers: joint report from a collaborative study | Beaudet, A; Bowcock, A; Buchwald, M; Cavalli-Sforza, L; Farrall, M; King, MC; Klinger, K; Lalouel, JM; Lathrop, G; Naylor, S; Ott, J; Tsui, LC; Wainwright, B; Watkins, P; White, R; Williamson, R | 1986 | 335 |
| Linkage of DNA probe B79a (D7S13) to cystic fibrosis | Wainwright, BJ; Tsui, LC; Leppert, M; Buchwald, M; Estivill, X; O'Connell, P; Lathrop, M; LaLouel, JM; White, R; Williamson, R; Farrall, M | 1987 | 268 |
| Linkage study of the dopamine D5 receptor gene and Gilles de la Tourette syndrome | Barr, CL; Wigg, KG; Zovko, E; Sandor, P; Tsui, L-C | 1997 | 193 |
| Localization of 67 exons on a YAC contig spanning 1.5 Mb around the multidrug resistance gene region of human chromosome 7q21.1 | Torigoe, K; Harada, T; Kusaba, H; Uchiumi, T; Kohno, K; Green, ED; Scherer, SW; Tsui, LC; Schlessinger, D; Kuwano, M; Wada, M | 1998 | 399 |
| Localization of a beta-crystallin gene, Hu beta A3/A1 (gene symbol:CRYB1), to the long arm of human chromosome 17 | Law, ML; Cai, GY; Hartz, J; Kao, FT; Hogg, D; Breitman, ML; Tsui, LC | 1986 | 224 |
| Localization of the gene encoding the α 2/δ-subunits of the L-type voltage dependent calcium channel to chromosome 7q and analysis of the segregation of flanking markers in malignant hyperthermia susceptible families | Iles, DE; LehmannHorn, F; Scherer, SW; Tsui, LC; Weghuis, DO; Suijkerbuijk, RF; Heytens, L; Mikala, G; Schwartz, A; Ellis, FR; Stewart, AD; Deufel, T; Wieringa, B | 1994 | 226 |
| Localization of the gene encoding the α2/δ subunit (CACNL2A) of the human skeletal muscle voltage-dependent Ca2+ channel to chromosome 7q21- q22 by somatic cell hybrid analysis | Powers, PA; Scherer, SW; Tsui, LC; Gregg, RG; Hogan, K | 1994 | 90 |
| Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis | Musarella, MA; Burghes, A; AnsonCartwright, L; Mahtani, MM; Argonza, R; Tsui, LC; Worton, R | 1988 | 218 |
| Localization of the human dihydrolipoamide dehydrogenase gene (DLD) to 7q31→q32 | Scherer, SW; Otulakowski, G; Robinson, BH; Tsui, LC | 1991 | 304 |
| Localization of the human gene encoding the 13.3-kDa subunit of mitochondrial complex III (UQCRB) to 8q22 by in situ hybridization | Malaney, S; Heng, HHQ; Tsui, LC; Shi, XM; Robinson, BH | 1996 | 243 |
| Localization of the human gene for inducible nitric oxide synthase (NOS2) to chromosome 17q11.2-q12 | Marsden, PA; Heng, HHQ; Duff, CL; Shi, XM; Tsui, LC; Hall, AV | 1994 | 117 |
| Localization of two metabotropic glutamate receptor genes, GRM3 and GRM8, to human chromosome 7q | Scherer, SW; Duvoisin, RM; Kuhn, R; Heng, HHQ; Belloni, E; Tsui, LC | 1996 | 203 |
| Localization to chromosome 7q36.1 of the human XRCC2 gene, determining sensitivity to DNA-damaging agents | Thacker, J; Tambini, CE; Simpson, PJ; Tsui, LC; Scherer, SW | 1995 | 215 |
| Loci of intestinal distress in cystic fibrosis knockout mice | Haston, CK; Tsui, LC | 2003 | 352 |
| Locus CFM1: a potential modifier of pancreatic disease in children with cystic fibrosis | Sontag, MK; Hokanson, JE; Marshall, JA; Corey, M; Zerbe, GO; Tsui, L-C; Zielenski, J; Accurso, FJ | 2003 | 276 |
| A locus for a human hereditary cataract is closely linked to the γ-crystallin gene family | Lubsen, NH; Renwick, JH; Tsui, LC | 1987 | 240 |
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