Establishing the identity of Anna Anderson Manahanpp9 - 10 Mark Stoneking, Terry Melton, Julian Nott, Suzanne Barritt, Rhonda Roby, Mitchell Holland, Victor Weedn, Peter Gill, Colin Kimpton, Rosemary Aliston-Greiner
& Kevin Sullivan doi:10.1038/ng0195-9 References|PDF
(364K)
Polymerase variants in RER colorectal tumourspp10 - 11 Luis T. da Costa, Bo Liu, Wafik S. El-Deiry, Stanley R. Hamilton, Kenneth W. Kinzler, Bert Vogelstein, Sanford Markowitz, James K.V. Willson, Albert de la Chapelle, Kathleen M. Downey
& Antero G. So doi:10.1038/ng0195-10 References|PDF
(369K)
Characteristics of imprinted genespp12 - 13 Bjorn Neumann, Pavel Kubicka
& Denise P. Barlow doi:10.1038/ng0195-12 References|PDF
(464K)
Genetic analysis of complex diseasep13 David Curtis, Pak C. Sham
& Homero P. Vallada doi:10.1038/ng0195-13 References|PDF
(96K)
The Sry-related gene Sox9 is expressed during chondrogenesis in mouse embryospp15 - 20 Edwina Wright, Murray R. Hargrave, Jeffrey Christiansen, Leanne Cooper, Jutta Kun, Timothy Evans, Uma Gangadharan, Andy Greenfield
& Peter Koopman doi:10.1038/ng0195-15 Abstract + references|PDF
(834K)
The Alzheimer's A peptide induces neurodegeneration and apoptotic cell death in transgenic micepp21 - 30 Frank M. LaFerla, Brad T. Tinkle, Charles J. Bieberich, Christian C. Haudenschild
& Gilbert Jay doi:10.1038/ng0195-21 Abstract + references|PDF
(1,736K)
Targeted mutation in the col5a2 gene reveals a regulatory role for type V collagen during matrix assemblypp31 - 36 Konstantinos Andrikopoulos, Xin Liu, Douglas R. Keene, Rudolf Jaenisch
& Francesco Ramirez doi:10.1038/ng0195-31 Abstract + references|PDF
(1,045K)
A progressive early onset cataract gene maps to human chromosome 17q24pp37 - 40 Marlene M. Armitage, Jane D. Kivlin
& Robert E. Ferrell doi:10.1038/ng0195-37 Abstract + references|PDF
(409K)
Functional inactivation but not structural mutation of p53 causes liver cancerpp41 - 47 Hiroyuki Ueda, Stephen J. Ullrich, J. David Gangemi, Catherine A. Kappel, Lien Ngo, Mark A. Feitelson
& Gilbert Jay doi:10.1038/ng0195-41 Abstract + references|PDF
(1,076K)
Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instabilitypp48 - 55 Bo Liu, Nicholas C. Nicolaides, Sanford Markowitz, James K.V. Willson, Ramon E. Parsons, Jin Jen, Nickolas Papadopolous, Päivi Peltomäki, Albert de la Chapelle, Stanley R. Hamilton, Kenneth W. Kinzler
& Bert Vogelstein doi:10.1038/ng0195-48 Abstract + references|PDF
(872K)
A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patientspp56 - 62 Terri G. Thompson, Christine J. DiDonato, Louise R. Simard, Susan E. Ingraham, Arthur H.M. Burghes, Thomas O. Crawford, Camille Rochette, Jerry R. Mendell
& John J. Wasmuth doi:10.1038/ng0195-56 Abstract + references|PDF
(897K)
A genetic linkage map of the laboratory rat, Rattus norvegicuspp63 - 69 Howard J. Jacob, Donna M. Brown, Ruth K. Bunker, Mark J. Daly, Victor J. Dzau, Alec Goodman, George Koike, Vladimir Kren, Theodore Kurtz, Åke Lernmark, Göran Levan, Yi-pei Mao, Anna Pettersson, Michal Pravenec, Jason S. Simon, Claude Szpirer, Josiane Szpirer, Maria R. Trolliet, Eric S. Winer
& Eric S. Lander doi:10.1038/ng0195-63 Abstract + references|PDF
(636K)
A germline insertion in the tuberous sclerosis (Tsc2) gene gives rise to the Eker rat model of dominantly inherited cancerpp70 - 74 Toshiyuki Kobayashi, Youko Hirayama, Etsuko Kobayashi, Yoshiaki Kubo
& Okio Hino doi:10.1038/ng0195-70 Abstract + references|PDF
(677K)
A mutation in the tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathypp75 - 79 Nigel G. Laing, Stephen D. Wilton, Patrick A. Akkari, Shellie Dorosz, Karyn Boundy, Chris Kneebone, Peter Blumbergs, Sue White, Hugh Watkins, Donald R. Love
& Eric Haan doi:10.1038/ng0195-75 Abstract + references|PDF
(549K)
Linkage disequilibrium mapping of a type 1 diabetes susceptibility gene (IDDM7) to chromosome 2q31−q33pp80 - 85 J.B. Copeman, F. Cucca, C.M. Hearne, R.J. Cornall, P.W. Reed, K.S. Rønningen, D.E. Undlien, L. Nisticò, R. Buzzetti, R. Tosi, F. Pociot, J. Nerup, F. Cornélis, A.H. Barnett, S.C. Bain
& J.A. Todd doi:10.1038/ng0195-80 Abstract + references|PDF
(651K)
A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17pp86 - 91 Thomas B. Friedman, Yong Liang, James L. Weber, John T. Hinnant, Thomas D. Barber, Sunaryana Winata, I. Nyoman Arhya
& James H. Asher Jr doi:10.1038/ng0195-86 Abstract + references|PDF
(876K)
Autosomal recessive ocular albinism associated with a functionally significant tyrosinase gene polymorphismpp92 - 95 Kazuyoshi Fukai, Stuart A. Holmes, Neil J. Lucchese, Victoria Mok Siu, Richard G. Weleber, Rhonda E. Schnur
& Richard A. Spritz doi:10.1038/ng0195-92 Abstract + references|PDF
(478K)
variants in RER colorectal tumours
peptide induces neurodegeneration and apoptotic cell death in transgenic mice
tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy
