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Title	Author(s)	Issue Date
A susceptibility locus for non-insulin-dependent diabetes mellitus (NIDDM) is located at 7q21 3-q221 Journal:Diabetes	Prochazka, M Thompson, DB Elbein, SC Scherer, SW Tsui, L-C Furlong, C Knowler, WC Bennett, PH Bogardus, C	1997
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia Journal:American Journal of Human Genetics	Feuk, L Kalervo, A LipsanenNyman, M Skaug, J Nakabayashi, K Finucane, B Hartung, D Innes, M Kerem, B Nowaczyk, MJ Rivlin, J Roberts, W Senman, L Summers, A Szatmari, P Wong, V Vincent, JB Zeesman, S Osborne, LR Cardy, JO Kere, J Scherer, SW HannulaJouppi, K	2006
Altered expression and deletion of RMO1 in osteosarcoma Journal:International Journal of Cancer	Eppert, K Wunder, JS Aneliunas, V Tsui, LC Scherer, SW Andrulis, IL	2005
Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactyly Journal:Human Genetics	Vargas, FR Roessler, E Gaudenz, K Belloni, E Whitehead, AS Kirke, PN Mills, JL Hooper, G Stevenson, RE Cordeiro, I Correia, P Felix, T Gereige, R Cunningham, ML Canún, S Antonarakis, SE Strachan, T Tsui, LC Scherer, SW Muenke, M	1998
Assignment of growth factor receptor-bound protein 10 (GRB10) to human chromosome 7p11.2-p12 Journal:Genomics	Jerome, CA Scherer, SW Tsui, LC Gietz, RD TriggsRaine, B	1997
Assignment of the 5-hydroxytryptamine (serotonin) receptor 5A gene (HTR5A) to human chromosome band 7q36.1 Journal:Cytogenetics and Cell Genetics	Schanen, NC Scherer, SW Tsui, LC Francke, U	1996
Assignment of the human homolog of mouse Dlx3 to Chromosome 17q21.3-q22 by analysis of somatic cell hybrids and fluorescence in situ hybridization Journal:Mammalian Genome	Scherer, SW Heng, HHQ Robinson, GW Mahon, KA Evans, JP Tsui, LC	1995
Assignment of the SLC25A12 gene coding for the human calcium-binding mitochondrial solute carrier protein aralar to human chromosome 2q24 Journal:Cytogenetics and Cell Genetics	Crackower, MA Sinasac, DS Lee, JR Herbrick, JA Tsui, LC Scherer, SW	1999
The BCL7 gene family: Deletion of BCL7B in Williams syndrome Journal:Gene	Jadayel, DM Osborne, LR Coignet, LJA Zani, VJ Tsui, LC Scherer, SW Dyer, MJS	1998
Characterization of the segmental duplication LCR7-20 in the human genome Journal:Genomics	Liu, X Li, X Li, M Acimovic, YJ Li, Z Scherer, SW Estivill, X Tsui, LC	2004
Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development Journal:Human Molecular Genetics	Crackower, MA Scherer, SW Rommens, JM Hui, CC Poorkaj, P Soder, S Cobben, JM Hudgins, L Evans, JP Tsui, LC	1996
Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome Journal:Human Molecular Genetics	Estivill, X Cheung, J Pujana, MA Nakabayashi, K Scherer, SW Tsui, LC	2002
Cloning and characterization of PDK4 on 7q21.3 encoding a fourth pyruvate dehydrogenase kinase isoenzyme in human Journal:Journal of Biological Chemistry	Rowles, J Scherer, SW Xi, T Majer, M Nickle, DC Rommens, JM Popov, KM Harris, RA Riebow, NL Xia, J Tsui, LC Bogardus, C Prochazka, M	1996
Cloning of a DSS1 pseudogene (DSS1P1) and mapping to human Chromosome band 5q14 Journal:Mammalian Genome	Crackower, MA Scherer, SW Heng, HHQ Tsui, LC	1997
Comparative analysis of the gene-dense ACHE/TFR2 region on human chromosome 7q22 with the orthologous region on mouse chromosome 5 Journal:Nucleic Acids Research	Wilson, MD Riemer, C Martindale, DW Schnupf, P Boright, AP Cheung, TL Hardy, DM Schwartz, S Scherer, SW Tsui, LC Miller, W Koop, BF	2001
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor Journal:Cell	Freund, CL GregoryEvans, CY Furukawa, T Papaioannou, M Looser, J Ploder, L Bellingham, J Ng, D Herbrick, JAS Duncan, A Scherer, SW Tsui, LC LoutradisAnagnostou, A Jacobson, SG Cepko, CL Bhattacharya, SS McInnes, RR	1997
Crosstalk between histone modification and DNA methylation in patients with intellectual disability syndrome due to JARID1C mutations Proceeding/Conference:Canadian Epigenetics Conference, Eh! 2011	Chung, BHY Grafodatskaya, D Butcher, DT Scherer, SW Abidi, FE Schwartz, CE Wekserg, R	2011
Crosstalk between histone modifications and DNA methylation in patients with intellectual disability due to JARID1C mutations Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2010	Chung, B Grafodatskaya, D Butcher, DT Scherer, SW Abidi, FE Schwartz, CE Weksberg, R	2010
Crosstalk between histone modifications and DNA methylation in patients with intellectual disability due to JARID1C mutations Proceeding/Conference:Annual Scientific Meeting of the Canadian College of Medical Geneticists, CCMG 2010	Chung, BHY Grafodatskaya, D Butcher, DT Scherer, SW Abidi, FE Schwartz, CE Weksberg, R	2010
Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly Journal:Human Genetics	Roessler, E Ward, DE Gaudenz, K Belloni, E Scherer, SW Donnai, D SiegelBartelt, J Tsui, LC Muenke, M	1997

Showing results 3 to 22 of 110 < previous next >