Gene therapy for cholesterolpp349 - 350 Michael S. Brown, Joseph L. Goldstein, Richard J. Havel
& Daniel Steinberg doi:10.1038/ng0794-349 References|PDF
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Complete mitochondrial genome amplificationpp350 - 351 Suzanne Cheng, Russell Higuchi
& Mark Stoneking doi:10.1038/ng0794-350 References|PDF
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The rumpshaker mutation in spastic paraplegiapp351 - 352 Hisashi Kobayashi, Eric P. Hoffman
& Harold G. Marks doi:10.1038/ng0794-351 References|PDF
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Tumour predisposition in mice heterozygous for a targeted mutation in Nf1pp353 - 361 Tyler Jacks, T. Shane Shih, Earlene M. Schmitt, Roderick T. Bronson, Andre Bernards
& Robert A. Weinberg doi:10.1038/ng0794-353 Abstract + references|PDF
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Inactivation of E2a in recombinant adenoviruses improves the prospect for gene therapy in cystic fibrosispp362 - 369 Yiping Yang, Frederick A. Nunes, Klara Berencsi, Eva Gönczöl, John F. Engelhardt
& James M. Wilson doi:10.1038/ng0794-362 Abstract + references|PDF
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Alterations in the PITSLRE protein kinase gene complex on chromosome 1p36 in childhood neuroblastomapp370 - 375 Jill M. Lahti, Marcus Valentine, Jialing Xiang, Bart Jones, Joseph Amann, Jose Grenet, Gail Richmond, A. Thomas Look
& Vincent J. Kidd doi:10.1038/ng0794-370 Abstract + references|PDF
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The distribution of CpG islands in mammalian chromosomespp376 - 382 Jeffrey M. Craig
& Wendy A. Bickmore doi:10.1038/ng0794-376 Abstract + references|PDF
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An ancient family of embryonically expressed mouse genes sharing a conserved protein motif with the T locuspp383 - 389 Roni J. Bollag, Zahava Siegfried, Judith A. Cebra-Thomas, Nancy Garvey, Ewa M. Davison
& Lee M. Silver doi:10.1038/ng0794-383 Abstract + references|PDF
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Chromosome−specific microsatellite sets for fluorescence−based, semi−automated genome mappingpp390 - 395 P. W. Reed, J. L. Davies, J. B. Copeman, S. T. Bennett, S. M. Palmer, L. E. Pritchard, S. C. L. Gough, Y. Kawaguchi, H. J. Cordell, K. M. Balfour, S. C. Jenkins, E. E. Powell, A. Vignal
& J. A. Todd doi:10.1038/ng0794-390 Abstract + references|PDF
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Germline mutations in the thyrotropin receptor gene cause non−autoimmune autosomal dominant hyperthyroidismpp396 - 401 Laurence Duprez, Jasmine Parma, Jacqueline Van Sande, Anouk Allgeier, Jacques Leclère, Claire Schvartz, Marie-Joëlle Delisle, Marc Decoulx, Jacques Orgiazzi, Jacques Dumont
& Gilbert Vassart doi:10.1038/ng0794-396 Abstract + references|PDF
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X−linked spastic paraplegia (SPG1), MASA syndrome and X−linked hydrocephalus result from mutations in the L1 genepp402 - 407 Monique Jouet, André Rosenthal, Giles Armstrong, John MacFarlane, Roger Stevenson, Joan Paterson, Aïda Metzenberg, Victor Ionasescu, Karen Temple
& Susan Kenwrick doi:10.1038/ng0794-402 Abstract + references|PDF
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MASA syndrome is due to mutations in the neural cell adhesion gene L1CAMpp408 - 413 Lieve Vits, Guy Van Camp, Paul Coucke, Erik Fransen, Kristel De Boulle, Edwin Reyniers, Bernhard Korn, Annemarie Poustka, Golder Wilson, Connie Schrander-Stumpel, Robin M. Winter, Charles Schwartz
& Patrick J. Willems doi:10.1038/ng0794-408 Abstract + references|PDF
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Highly homologous loci on the X and Y chromosomes are hot−spots for ectopic recombinations leading to XX malenesspp414 - 419 Dominique Weil, Irène Wang, Alexander Dietrich, Annemarie Poustka, Jean Weissenbach
& Christine Petit doi:10.1038/ng0794-414 Abstract + references|PDF
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High resolution localization of recombination hot spots using sperm typingpp420 - 424 Rene Hubert, Marcy MacDonald, James Gusella
& Norman Arnheim doi:10.1038/ng0794-420 Abstract + references|PDF
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Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33−q35pp425 - 428 Afif Hentati, Khemissa Bejaoui, Margaret A. Pericak-Vance, Faycal Hentati, Marcy C. Speer, Wu-Yen Hung, Denise A. Figlewicz, Jonathan Haines, Jackie Rimmler, Christiane Ben Hamida, Mongi Ben Hamida, Robert H. Brown Jr
& Teepu Siddique doi:10.1038/ng0794-425 Abstract + references|PDF
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Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21−cenpp429 - 432 K. Zerres, G. Mücher, L. Bachner, G. Deschennes, T. Eggermann, H. Kääriäinen, M. Knapp, T. Lennert, J. Misselwitz, K. E. von Mühlendahl, H. P. H. Neumann, Y. Pirson, S. Rudnik-Schöneborn, V. Steinbicker, B. Wirth
& K. Schärer doi:10.1038/ng0794-429 Abstract + references|PDF
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Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumourpp433 - 439 Marja J. C. Steenman, Shirley Rainier, Craig J. Dobry, Paul Grundy, Isabelle L. Horon
& Andrew P. Feinberg doi:10.1038/ng0794-433 Abstract + references|PDF
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Epigenetic lesions at the H19 locus in Wilms' tumour patientspp440 - 447 Thomas Moulton, Taria Crenshaw, Yue Hao, Josh Moosikasuwan, Na Lin, Francine Dembitzer, Terrence Hensle, Lawrence Weiss, Lydia McMorrow, Thomas Loew, Wilma Kraus, William Gerald
& Benjamin Tycko doi:10.1038/ng0794-440 Abstract + references|PDF
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