| Title | Author(s) | Year | View Count |
 | Human chromosome 7: DNA sequence and biology | Scherer, SW; Cheung, J; MacDonald, JR; Osborne, LR; Nakabayashi, K; Herbrick, JA; Carson, AR; ParkerKatiraee, L; Skaug, J; Khaja, R; Zhang, J; Hudek, AK; Li, M; Haddad, M; Duggan, GE; Fernandez, BA; Kanematsu, E; Gentles, S; Christopoulos, CC; Choufani, S; Kwasnicka, D; Zheng, XH; Lai, Z; Nusskern, D; Zhang, Q; Gu, Z; Lu, F; Zeesman, S; Nowaczyk, MJ; Teshima, I; Chitayat, D; Shuman, C; Weksberg, R; Zackai, EH; Grebe, TA; Cox, SR; Kirkpatrick, SJ; Rahman, N; Friedman, JM; Heng, HHQ; Pelicci, PG; LoCoco, F; Belloni, E; Shaffer, LG; Pober, B; Morton, CC; Gusella, JF; Bruns, GAP; Korf, BR; Quade, BJ; Ligon, AH; Ferguson, H; Higgins, AW; Leach, NT; Herrick, SR; Lemyre, E; Farra, CG; Kim, HG; Summers, AM; Gripp, KW; Roberts, W; Szatmari, P; Winsor, EJT; Grzeschik, KH; Teebi, A; Minassian, BA; Kere, J; Armengol, L; Pujana, MA; Estivill, X; Wilson, MD; Koop, BF; Tosi, S; Moore, GE; Boright, AP; Zlotorynski, E; Kerem, B; Kroisel, PM; Petek, E; Oscier, DG; Mould, SJ; Döhner, H; Döhner, K; Rommens, JM; Vincent, JB; Venter, JC; Li, PW; Mural, RJ; Adams, MD; Tsui, LC | 2003 | 677 |
 | Circling, deafness and yellow coat displayed by chromosome 3 mouse mutants yellow submarien (Ysb) and light coat and circling (Lcc) | Pelling, AL; Leung, KKH; Dong, S; Lee, YT; Tang, ASP; Heng, HHQ; Tsui, LC; Tease, C; Fisher, G; Steel, KP; Cheah, KSE | 2002 | 198 |
| Circling, deafness, and yellow coat displayed by yellow submarine (Ysb) and light coat and circling (Lcc) mice with mutations on chromosome 3 | Dong, S; Leung, KKH; Pelling, AL; Lee, PYT; Tang, ASP; Heng, HHQ; Tsui, LC; Tease, C; Fisher, G; Steel, KP; Cheah, KSE | 2002 | 375 |
| Assignment of the gene encoding the limbic system-associated membrane protein (LAMP) to mouse chromosome 16B5 and human chromosome 3q13.2-q21 | Pimenta, AF; Tsui, LC; Heng, HHQ; Levitt, P | 1998 | 90 |
| High resolution free chromatin/DNA fiber fluorescent in situ hybridization | Heng, HHQ; Tsui, LC | 1998 | 80 |
| Assignment of mouse fibroblast growth factor 10 (Fgf10) gene to the telomeric region of chromosome 13 | Crackower, MA; Heng, HHQ; Tsui, LC | 1998 | 110 |
| 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 | 94 |
| Assignment of the human dUTPase gene (DUT) to chromosome 15q15-q21.1 by fluorescence in situ hybridization | Cohen, D; Heng, HHQ; Shi, XM; McIntosh, EM; Tsui, LC; Pearlman, RE | 1997 | 145 |
| Cloning of a DSS1 pseudogene (DSS1P1) and mapping to human Chromosome band 5q14 | Crackower, MA; Scherer, SW; Heng, HHQ; Tsui, LC | 1997 | 108 |
| Specific and redundant functions of Gli2 and Gli3 zinc finger genes in skeletal patterning and development | Mo, R; Freer, AM; Zinyk, DL; Crackower, MA; Michaud, J; Heng, HHQ; Chik, KW; Shi, XM; Tsui, LC; Cheng, SH; Joyner, AL; Hui, CC | 1997 | 162 |
| Expression analysis and chromosomal assignment of the human SFRS5/SRp40 gene | Snow, BE; Heng, HHQ; Shi, XM; Zhou, Y; Du, K; Taub, R; Tsui, LC; McInnes, RR | 1997 | 385 |
| PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7 | Osborne, LR; Herbrick, JA; Greavette, T; Heng, HHQ; Tsui, LC; Scherer, SW | 1997 | 213 |
| Amplification of CFTR exon 9 sequences to multiple locations in the human genome | Rozmahel, R; Heng, HHQ; Duncan, AMV; Shi, XM; Rommens, JM; Tsui, LC | 1997 | 285 |
| Identification and characterization of human genes encoding Hprp3p and Hprp4p, interacting components of the spliceosome | Wang, A; FormanKay, J; Luo, Y; Luo, M; Chow, YH; Plumb, J; Friesen, JD; Tsui, LC; Heng, HHQ; Woolford Jr, JL; Hu, J | 1997 | 364 |
| Cloning, expression, and chromosomal localization to 11p12-13 of a human LIM/HOMEOBOX gene, hLim-1 | Dong, WF; Heng, HHQ; Lowsky, R; Xu, Y; DeCoteau, JF; Shi, XM; Tsui, L-C; Minden, MD | 1997 | 322 |
| Chromosomal mapping of the second human CD8B gene locus | Zhang, XL; Heng, HHQ; Yang, Y; Tsui, LC; Parnes, JR; Chamberlain, JW | 1996 | 67 |
| Identification of a human LIM-Hox gene, hLH-2, aberrantly expressed in chronic myelogenous leukaemia and located on 9q33-34.1 | Wu, HK; Heng, HHQ; Siderovski, DP; Dong, WF; Okuno, Y; Shi, XM; Tsui, LC; Minden, MD | 1996 | 123 |
| Direct detection of expanded trinucleotide repeats using PCR and DNA hybridization techniques | Petronis, A; Heng, HHQ; Tatuch, Y; Shi, XM; Klempan, TA; Tsui, LC; Ashizawa, T; Surh, LC; Holden, JJA; Kennedy, JL | 1996 | 245 |
| 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 | 202 |
| Regulation of meiotic chromatin loop size by chromosomal position | Heng, HHQ; Chamberlain, JW; Shi, XM; Spyropoulos, B; Tsui, LC; Moens, PB | 1996 | 203 |
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