@article {Kipling:1997:0964-6906:1999, author = "Kipling, David", title = "Mammalian Telomerase: Catalytic Subunit and Knockout Mice", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "1999-2004", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00001" } @article {Andrew:1997:0964-6906:2005, author = "Andrew, Susan E. and Goldberg, Y. Paul and Hayden, Michael R.", title = "Rethinking Genotype and Phenotype Correlations in Polyglutamine Expansion Disorders", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2005-2010", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00002" } @article {Kilian:1997:0964-6906:2011, author = "Kilian, Andrzej and Bowtell, David D.L. and Abud, Helen E. and Hime, Gary R. and Venter, Deon J. and Keese, Paul K. and Duncan, Emma L. and Reddel, Roger R. and Jefferson, Richard A.", title = "Isolation of a Candidate Human Telomerase Catalytic Subunit Gene, Which Reveals Complex Splicing Patterns in Different Cell Types", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2011-2019", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00003" } @article {Qian:1997:0964-6906:2021, author = "Qian, Naifeng and Frank, Dale and O'Keefe, Denise and Dao, Diem and Zhao, Long and Yuan, Luwa and Wang, Qing and Keating, Mark and Walsh, Colum and Tycko, Benjamin", title = "The IPL Gene on Chromosome 11p15.5 is Imprinted in Humans and Mice and is Similar to TDAG51, Implicated in Fas Expression and Apoptosis", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2021-2029", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00004" } @article {Heckel:1997:0964-6906:2031, author = "Heckel, Dirk and Brass, Nicole and Fischer, Ulrike and Blin, Nikolaus and Steudel, Ingo and Tureci, Ozlem and Fackler, Oliver and Zang, Klaus D. and Meese, Eckart", title = "cDNA Cloning and Chromosomal mapping of a Predicted Coiled-Coil Proline-Rich Protein Immunogenic in Meningioma Patients", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2031-2041", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00005" } @article {Brodsky:1997:0964-6906:2043, author = "Brodsky, Gary and Barnes, Tristan and Bleskan, John and Becker, Laurence and Cox, Marlin and Patterson, David", title = "The Human GARS-AIRS-GART Gene Encodes Two Proteins Which Are Differentially Expressed during Human Brain Development and Temporally Overexpressed in Cerebellum of Individuals with Down Dyndrome", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2043-2050", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00006" } @article {Drouin:1997:0964-6906:2051, author = "Drouin, Regen and Angers, Martin and Dallaire, Nancy and Rose, Timothy M. and Khandjian, Edouard W. and Rousseau, Francois", title = "Structural and Functional Characterization of the Human FMR1 Promoter Reveals Similarities with the hnRNP-A2 Promoter Region", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2051-2060", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00007" } @article {Harland:1997:0964-6906:2061, author = "Harland, Mark and Meloni, Rolando and Gruis, Nelleke and Pinney, Elizabeth and Brookes, Sharon and Spurr, Nigel K. and Frischauf, Anna-Marie and Bataille, Veronique and Peters, Gordon and Cuzick, Jack and Selby, Peter and Bishop, D. Timothy and Bishop, Julia Newton", title = "Germline Mutations of the CDKN2 Gene in UK Melanoma Families", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2061-2067", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00008" } @article {Laitinen:1997:0964-6906:2069, author = "Laitinen, Tarja and Kauppi, Paula and Ignatius, Jaakko and Ruotsalainen, Tarja and Daly, Mark J. and Kaariainen, Helena and Kruglyak, Leonid and Laitinen, Hannu and de la Chapelle, Albert and Lander, Eric S. and Laitinen, Lauri A. and Kere, Juha", title = "Genetic Control of Serum IgE Levels and Asthma: Linkage and Linkage Disequilibrium Studies in an Isolated Population", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2069-2076", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00009" } @article {Julier:1997:0964-6906:2077, author = "Julier, Cecile and Delepine, Marc and Keavney, Bernard and Terwilliger, Joseph and Davis, S. and Weeks, Daniel E. and Bui, Thuan and Jeunemaitre, Xavier and Velho, Gilberto and Froguel, Philippe and Ratcliffe, Peter and Corvol, Pierre and Soubrier, Florent and Mark Lathrop, G.", title = "Genetic Susceptibility for Human Familial Essential Hypertension in a Region of Homology with Blood Pressure Linkage on Rat Chromosome 10", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2077-2085", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00010" } @article {Eckman:1997:0964-6906:2087, author = "Eckman, Christopher B. and Mehta, Nitin D. and Crook, Richard and Perez-tur, Jordi and Prihar, Guy and Pfeiffer, Eric and Graff-Radford, Neill and Hinder, Paul and Yager, Debra and Zenk, Brenda and Refolo, Lawrence M. and Mihail Prada, Cristian and Younkin, Steven G. and Hutton, Mike and Hardy, John", title = "A New Pathogenic Mutation in the APP Gene (I716V) Increases the Relative Proportion of A42(43)", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2087-2089", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00011" } @article {Adam:1997:0964-6906:2091, author = "Adam, Marie F. and Belmouden, Ahmed and Binisti, Philippe and Brezin, Antoine P. and Valtot, Francoise and Bechetoille, Alain and Dascotte, Jean-Claude and Copin, Bruno and Gomez, Lucienne and Chaventre, Andre and Bach, Jean-Francois and Garchon, Henri-Jean", title = "Recurrent Mutations in a Single Exon Encoding the Evolutionarily Conserved Olfactomedin-Homology Domain of TIGR in Familial Open-Angle Glaucoma", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2091-2097", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00012" } @article {Mak:1997:0964-6906:2099, author = "Mak, Victor and Jarvi, Keith A. and Zielenski, Julian and Durie, Peter and Tsui, Lap-Chee", title = "Higher Proportion of Intact Exon 9 CFTR mRNA in Nasal Epithelium Compared with Vas Deferens", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2099-2107", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00013" } @article {Semina:1997:0964-6906:2109, author = "Semina, Elena V. and Reiter, Rebecca S. and Murray, Jeffrey C.", title = "Isolation of a New Homeobox Gene Belonging to the Pitx/Rieg Family: Expression During Lens Development and Mapping to the Aphakia Region on Mouse Chromosome 19", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2109-2116", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00014" } @article {Wang:1997:0964-6906:2117, author = "Wang, Anan and Forman-Kay, Julie and Luo, Yu and Luo, Ming and Chow, Yu-Hua and Plumb, Jonathan and Friesen, James D. and Tsui, Lap-Chee and Heng, Henry H. Q. and Woolford, John L. and Hu, Jim", title = "Identification and Characterization of Human Genes Encoding Hprp3p and Hprp4p, Interacting Components of the Spliceosome", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2117-2126", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00015" } @article {Meguro:1997:0964-6906:2127, author = "Meguro, Makiko and Mitsuya, Kohzoh and Sui, Hajime and Shigenami, Katsuyo and Kugoh, Hiroyuki and Nakao, Mitsuyoshi and Oshimura, Mitsuo", title = "Evidence for Uniparental, Paternal Expression of the Human GABAA Receptor Subunit Genes, Using Microcell-Mediated Chromosome Transfer", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2127-2133", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00016" } @article {Kaytor:1997:0964-6906:2135, author = "Kaytor, Michael D. and Burright, Eric N. and Duvick, Lisa A. and Zoghbi, Huda Y. and Orr, Harry T.", title = "Increased Trinucleotide Repeat Instability with Advanced Maternal Age", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2135-2139", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00017" } @article {Sathasivam:1997:0964-6906:2141, author = "Sathasivam, Kirupa and Baxendale, Sarah and Mangiarini, Laura and Bertaux, Fabien and Hetherington, Colin and Kanazawa, Ichiro and Lehrach, Hans and Bates, Gillian P.", title = "Aberrant Processing of the Fugu HD (FrHD) mRNA in Mouse Cells and in Transgenic Mice", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2141-2149", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00018" } @article {Lambert:1997:0964-6906:2151, author = "Lambert, Jean-Charles and Perez-Tur, Jordi and Dupire, Marie-Joelle and Galasko, Douglas and Mann, David and Amouyel, Philippe and Hardy, John and Delacourte, Andre and Chartier-Harlin, Marie-Christine", title = "Distortion of Allelic Expression of Apolipoprotein E in Alzheimer's Disease", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2151-2154", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00019" } @article {Jones:1997:0964-6906:2155, author = "Jones, Alistair C. and Daniells, Claire E. and Snell, Russell G. and Tachataki, Maria and Idziaszczyk, Shelley A. and Krawczak, Michael and Sampson, Julian R. and Cheadle, Jeremy P.", title = "Molecular Genetic and Phenotypic Analysis Reveals Differences between TSC1 and TSC2 Associated Familial and Sporadic Tuberous Sclerosis", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2155-2161", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00020" } @article {Carrasquillo:1997:0964-6906:2163, author = "Carrasquillo, Minerva M. and Zlotogora, Joel and Barges, Saleh and Chakravarti, Aravinda", title = "Two Different Connexin 26 Mutations in an Inbred Kindred Segregating Non-Syndromic Recessive Deafness: Implications for Genetic Studies in Isolated Populations", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2163-2172", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00021" } @article {Denoyelle:1997:0964-6906:2173, author = "Denoyelle, Francoise and Weil, Dominique and Maw, Marion A. and Wilcox, Stephen A. and Lench, Nicholas J. and Allen-Powell, Denise R. and Osborn, Amelia H. and Dahl, Hans-Henrik M. and Middleton, Anna and Houseman, Mark J. and Dode, Catherine and Marlin, Sandrine and Boulila-ElGaied, Amel and Grati, Mohammed and Ayadi, Hammadi and BenArab, Saida and Bitoun, Pierre and Lina-Granade, Genevieve and Godet, Jacqueline and Mustapha, Mirna and Loiselet, Jacques and El-Zir, Elie and Aubois, Anne and Joannard, Alain and Levilliers, Jacqueline and Garabedian, Erea-Noel and Mueller, Robert F. and McKinlay Gardner, R. J. and Petit, Christine", title = "Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2173-2177", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00022" } @article {Tyson:1997:0964-6906:2179, author = "Tyson, Jessica and Tranebjaerg, Lisbeth and Bellman, Sue and Wren, Christopher and Taylor, James F.N. and Bathen, Jorn and Aslaksen, Bjorn and Sorland, Svein Jan and Lund, Ole and Malcolm, Sue and Pembrey, Marcus and Bhattacharya, Shomi and Bitner-Glindzicz, Maria", title = "IsK and KvLQT1: Mutation in Either of the Two Subunits of the Slow Component of the Delayed Rectifier Potassium Channel Can Cause Jervell and Lange-Nielsen Syndrome", journal = "Human Molecular Genetics", volume = "6", number = "12", year = "1997", pages = "2179-2185", url = "http://www.ingentaconnect.com/content/oup/hmg/1997/00000006/00000012/art00023" }