Results 1 to 20 of 48
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TypeTitleAuthor(s)YearViews
Human chromosome 7: DNA sequence and biologyScherer, 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, LC2003693
 
Circling, deafness, and yellow coat displayed by yellow submarine (Ysb) and light coat and circling (Lcc) mice with mutations on chromosome 3Dong, S; Leung, KKH; Pelling, AL; Lee, PYT; Tang, ASP; Heng, HHQ; Tsui, LC; Tease, C; Fisher, G; Steel, KP; Cheah, KSE2002375
 
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, KSE2002168
 
High resolution free chromatin/DNA fiber fluorescent in situ hybridizationHeng, HHQ; Tsui, LC1998136
 
Assignment of mouse fibroblast growth factor 10 (Fgf10) gene to the telomeric region of chromosome 13Crackower, MA; Heng, HHQ; Tsui, LC199898
 
Assignment of the gene encoding the limbic system-associated membrane protein (LAMP) to mouse chromosome 16B5 and human chromosome 3q13.2-q21Pimenta, AF; Tsui, LC; Heng, HHQ; Levitt, P1998105
 
Assignment of the human dUTPase gene (DUT) to chromosome 15q15-q21.1 by fluorescence in situ hybridizationCohen, D; Heng, HHQ; Shi, XM; McIntosh, EM; Tsui, LC; Pearlman, RE1997135
 
PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7Osborne, LR; Herbrick, JA; Greavette, T; Heng, HHQ; Tsui, LC; Scherer, SW1997224
 
Amplification of CFTR exon 9 sequences to multiple locations in the human genomeRozmahel, R; Heng, HHQ; Duncan, AMV; Shi, XM; Rommens, JM; Tsui, LC1997269
 
Expression analysis and chromosomal assignment of the human SFRS5/SRp40 geneSnow, BE; Heng, HHQ; Shi, XM; Zhou, Y; Du, K; Taub, R; Tsui, LC; McInnes, RR1997409
 
Fluorescent in situ mapping of the murine deleted in split hand/split foot 1 (dss1) gene to Chromosome 6Crackower, MA; Heng, HHQ; Shi, X; Scherer, SW; Tsui, LC199779
 
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
 
Cloning, expression, and chromosomal localization to 11p12-13 of a human LIM/HOMEOBOX gene, hLim-1Dong, WF; Heng, HHQ; Lowsky, R; Xu, Y; DeCoteau, JF; Shi, XM; Tsui, L-C; Minden, MD1997344
 
Cloning of a DSS1 pseudogene (DSS1P1) and mapping to human Chromosome band 5q14Crackower, MA; Scherer, SW; Heng, HHQ; Tsui, LC1997101
 
Specific and redundant functions of Gli2 and Gli3 zinc finger genes in skeletal patterning and developmentMo, R; Freer, AM; Zinyk, DL; Crackower, MA; Michaud, J; Heng, HHQ; Chik, KW; Shi, XM; Tsui, LC; Cheng, SH; Joyner, AL; Hui, CC1997156
 
Direct detection of expanded trinucleotide repeats using PCR and DNA hybridization techniquesPetronis, A; Heng, HHQ; Tatuch, Y; Shi, XM; Klempan, TA; Tsui, LC; Ashizawa, T; Surh, LC; Holden, JJA; Kennedy, JL1996239
 
Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patientsOsborne, LR; Martindale, D; Scherer, SW; Shi, XM; Huizenga, J; Heng, HHQ; Costa, T; Pober, B; Lew, L; Brinkman, J; Rommens, J; Koop, B; Tsui, LC1996284
 
Chromosomal mapping of the second human CD8B gene locusZhang, XL; Heng, HHQ; Yang, Y; Tsui, LC; Parnes, JR; Chamberlain, JW199675
 
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, MD1996119
 
Localization of two metabotropic glutamate receptor genes, GRM3 and GRM8, to human chromosome 7qScherer, SW; Duvoisin, RM; Kuhn, R; Heng, HHQ; Belloni, E; Tsui, LC1996178
 
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