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Showing results 37 to 56 of 110 < previous next >

Title	Author(s)	Issue Date
The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein Journal:Nature Genetics	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
Gene structure and chromosome localization to 7q21.3 of the human rod photoreceptor transducin γ-subunit gene (GNGT1) Journal:Genomics	Scherer, SW Feinstein, DS Oliveira, L Tsui, LC Pittler, SJ	1996
Gene structure of the human MET proto-oncogene Journal:Oncogene	Duh, FM Scherer, SW Tsui, LC Lerman, MI Zbar, B Schmidt, L	1997
Generation and chromosome mapping of expressed sequence tags (ESTs) from a human infant thymus Journal:Genome	Hwang, MY Kang, YJ Kim, YH Scherer, SW Tsui, LC Sohn, U	1999
Genetic variation in paraoxonase-1 and paraoxonase-2 is associated with variation in plasma lipoproteins in Alberta Hutterites Journal:Atherosclerosis	Boright, AP Connelly, PW Brunt, JH Scherer, SW Tsui, LC Hegele, RA	1998
Genetic variation in paraoxonase-2 is associated with variation in plasma lipoproteins in Canadian Oji-Cree Journal:Clinical Genetics	Hegele, RA Harris, SB Connelly, PW Hanley, AJG Tsui, LC Zinman, B Scherer, SW	1998
Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence. Journal:Genome biology	Cheung, J Estivill, X Khaja, R MacDonald, JR Lau, K Tsui, LC Scherer, SW	2003
Genomic structure of the adult-onset type II citrullinemia gene, SLC25A13, and cloning and expression of its mouse homologue Journal:Genomics	Sinasac, DS Crackower, MA Lee, JR Kobayashi, K Saheki, T Scherer, SW Tsui, LC	1999
Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas Journal:Nature genetics	Schmidt, L Duh, FM Chen, F Kishida, T Glenn, G Choyke, P Scherer, SW Zhuang, Z Lubensky, I Dean, M Allkimets, R Chidambaram, A Bergerheim, UR Feltis, JT Casadevall, C Zamarron, A Bernues, M Richard, S Lips, CJM Walther, MM Tsui, L-C Geil, L Orcutt, ML Stackhouse, T Lipan, J Slife, L Brauch, H Decker, J Niehans, G Hughson, MD Moch, H Storkel, S Lerman, MI Linehan, WM Zbar, B	1997
Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome: Letters to the editor	Osborne, LR Soder, S Shi, XM Pober, B Costa, T Scherer, SW Tsui, L-C	1997
Heterogeneity of the autosomal dominant split hand/split foot malformation [6] Journal:American Journal of Human Genetics	Zlotogora, J Evans, JP Palmer, S Scherer, SW Kukolich, M Wijsman, EM Tsui, LC Stephens, K	1995
A human Chromosome 7-specific genomic DNA library in yeast artificial chromosomes Journal:Mammalian Genome	Scherer, SW Tompkins, BJF Tsui, LC	1992
Human chromosome 7: DNA sequence and biology Journal:Science	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
Human Genome Variation 2006: emerging views on structural variation and large-scale SNP analysis Journal:Nature Genetics	Abecasis, G Tam, PKH Bustamante, CD Ostrander, EA Scherer, SW Chanock, SJ Kwok, PY Brookes, AJ	2007
The human metabotropic glutamate receptor 8 (GRM8) gene: A disproportionately large gene located at 7q31.3-q32.1 Journal:Genomics	Scherer, SW Soder, S Duvoisin, RM Huizenga, JJ Tsui, LC	1997
Human PON2 gene at 7q21.3: Cloning, multiple mRNA forms, and missense polymorphisms in the coding sequence Journal:Gene	Mochizuki, H Scherer, SW Xi, T Nickle, DC Majer, M Huizenga, JJ Tsui, LC Prochazka, M	1998
Identification of a 1300 kilobase deletion unit on chromosome 7q31.3 in invasive epithelial ovarian carcinomas Journal:Oncogene	Edelson, MI Scherer, SW Tsui, LC Welch, WR Bell, DA Berkowitz, RS Mok, SC	1997
Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome Journal:Genomics	Osborne, LR Campbell, T Daradich, A Scherer, SW Tsui, LC	1999
Identification of a yeast artificial chromosome clone spanning a translocation breakpoint at 7q32.1 in a Smith-Lemli-Opitz syndrome patient Journal:American Journal of Human Genetics	Alley, TL Gray, BA Lee, SH Scherer, SW Tsui, LC Tint, GS Williams, CA Zori, R Wallace, MR	1995
Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients Journal:Genomics	Osborne, LR Martindale, D Scherer, SW Shi, XM Huizenga, J Heng, HHQ Costa, T Pober, B Lew, L Brinkman, J Rommens, J Koop, B Tsui, LC	1996

Showing results 37 to 56 of 110 < previous next >