Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmiaspp17 - 23 Q. Wang, M.E. Curran, I. Splawski, T.C. Burn, J.M. Millholland, T.J. VanRaay, J. Shen, K.W. Timothy, G.M. Vincent, T. de Jager, P.J. Schwartz, J.A. Towbin, A.J. Moss, D.L. Atkinson, G.M. Landes, T.D. Connors
& M.T. Keating doi:10.1038/ng0196-17 Abstract + references|PDF
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Gitelman's variant of Barter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na−Cl cotransporterpp24 - 30 David B. Simon, Carol Nelson-Williams, Margaret Johnson Bia, David Ellison, Fiona E. Karet, Antonio Morey Molina, Ivar Vaara, Fujihiko Iwata, Howard M. Cushner, Marianne Koolen, Francisco J. Gainza, Hillel J. Gitelman
& Richard P. Lifton doi:10.1038/ng0196-24 Abstract + references|PDF
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Genetic analysis of non-insulin dependent diabetes mellitus in the GK ratpp31 - 37 Joakim Galli, Luo-Sheng Li, Anna Glaser, Claes-Göran Östenson, Hong Jiao, Hossein Fakhrai-Rad, Howard J. Jacob, Eric S. Lander
& Holger Luthman doi:10.1038/ng0196-31 Abstract + references|PDF
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Chromosomal mapping of genetic loci associated with non-insulin dependent diabetes in the GK ratpp38 - 43 Dominique Gauguier, Philippe Froguel, Véronique Parent, Catherine Bernard, Marie-Thérèse Bihoreau, Bernard Portha, Michael R. James, Luc Penicaud, Mark Lathrop
& Alain Ktorza doi:10.1038/ng0196-38 Abstract + references|PDF
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Renal disease susceptibility and hypertension are under independent genetic control in the fawn-hooded ratpp44 - 51 Donna M. Brown, Abraham P. Provoost, Mark J. Daly, Eric S. Lander
& Howard J. Jacob doi:10.1038/ng0196-44 Abstract + references|PDF
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Sjögren−Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase genepp52 - 57 Vincenzo De Laurenzi, Geraldine R. Rogers, David J. Hamrock, Lyuben N. Marekov, Peter M. Steinert, John G. Compton, Nelli Markova
& William B. Rizzo doi:10.1038/ng0196-52 Abstract + references|PDF
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Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approachpp58 - 64 Jamie E. Craig, Jacques Rochette, Chris A. Fisher, David J. Weatherall, Sophie Marc, G. Mark Lathrop, Florence Demenais
& SweeLay Thein doi:10.1038/ng0196-58 Abstract + references|PDF
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Selective capture of acentric fragments by micronuclei provides a rapid method for purifying extrachromosomally amplified DNApp65 - 71 Noriaki Shimizu, Teru Kanda
& Geoffrey M. Wahl doi:10.1038/ng0196-65 Abstract + references|PDF
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A protein linkage map of Escherichia coli bacteriophage T7pp72 - 77 Paul L. Bartel, Jennifer A. Roecklein, Dhruba SenGupta
& Stanley Fields doi:10.1038/ng0196-72 Abstract + references|PDF
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Dopamine D4 receptor (D4DR) exon III polymorphism associated with the human personality trait of Novelty Seekingpp78 - 80 Richard P. Ebstein, Olga Novick, Roberto Umansky, Beatrice Priel, Yamima Osher, Darren Blaine, Estelle R. Bennett, Lubov Nemanov, Miri Katz
& Robert H. Belmaker doi:10.1038/ng0196-78 Abstract + references|PDF
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Population and familial association between the D4 dopamine receptor gene and measures of Novelty Seekingpp81 - 84 Jonathan Benjamin, Lin Li, Chavis Patterson, Benjamin D. Greenberg, Dennis L. Murphy
& Dean H. Hamer doi:10.1038/ng0196-81 Abstract + references|PDF
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A two-hit model for developmental defects in Gorlin syndromepp85 - 87 Sonja Levanat, Robert J. Gorlin, Shari Fallet, Dennis R. Johnson, John E. Fantasia
& Alien E. Bale doi:10.1038/ng0196-85 Abstract + references|PDF
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Nonsense mutation in the human growth hormone-releasing hormone receptor causes growth failure analogous to the little (lit) mousepp88 - 90 Michael P. Wajnrajch, Joseph M. Gertner, Madeleine D. Harbison, Streamson C. Chua Jr.
& Rudolph L. Leibel doi:10.1038/ng0196-88 Abstract + references|PDF
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The fragile X mental retardation protein is associated with ribosomespp91 - 93 Edouard W. Khandjian, François Corbin, Stephane Woerly
& François Rousseau doi:10.1038/ng0196-91 Abstract + references|PDF
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Germline mutations in the homeobox gene EMX2 in patients with severe schizencephalypp94 - 96 Silvia Brunelli, Antonio Faiella, Valeria Capra, Vincenzo Nigro, Antonio Simeone, Armando Cama
& Edoardo Boncinelli doi:10.1038/ng0196-94 Abstract + references|PDF
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Germline mutations in the p16INK4a binding domain of CDK4 in familial melanomapp97 - 99 Lin Zuo, John Weger, Qingbei Yang, Alisa M. Goldstein, Margaret A. Tucker, Graeme J. Walker, Nicholas Hayward
& Nicholas C. Dracopoli doi:10.1038/ng0196-97 Abstract + references|PDF
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Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter genepp100 - 102 Andrea Superti-Furga, Johanna Hästbacka, William R. Wilcox, Daniel H. Cohn, Hans J. van der Harten, Antonio Rossi, Nenad Blau, David L. Rimoin, Beat Steinmann, Eric S. Lander
& Richard Gitzelmann doi:10.1038/ng0196-100 Abstract + references|PDF
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A mutation in the gene encoding the 2 chain of the fibril-associated collagen IX, COL9A2, causes multiple epiphyseal dysplasia (EDM2)pp103 - 105 Yasuteru Muragaki, Edwin C.M. Mariman, Sylvia E.C. van Beersum, Merja Perälä, Jan B.A. van Mourik, Matthew L. Warman, Bjorn R. Olsen
& Ben C.J. Hamel doi:10.1038/ng0196-103 Abstract + references|PDF
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Early neonatal death in mice homozygous for a null allele of the insulin receptor genepp106 - 109 Domenico Accili, John Drago, Eric J. Lee, Mark D. Johnson, Martha H. Cool, Paola Salvatore, Laureano D. Asico, Pedro A. José, Simeon I. Taylor
& Heiner Westphal doi:10.1038/ng0196-106 Abstract + references|PDF
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Corrigendum: A site-directed chromosomal translocation induced in embryonic stem cells by Cre-loxP recombinationp110 doi:10.1038/ng0196-110a PDF
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Corrigendum: Epileptic seizures caused by inactivation of a novel gene, jerky, related to centromere binding protein-B in transgenic micep110 doi:10.1038/ng0196-110b PDF
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Corrigendum: The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individualsp110 doi:10.1038/ng0196-110c PDF
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Corrigendum: -sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complexp110 doi:10.1038/ng0196-110d PDF
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2 chain of the fibril-associated collagen IX, COL9A2, causes multiple epiphyseal dysplasia (EDM2)
-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex
