HEAT repeats in the Huntington's disease proteinpp115 - 116 Miguel A. Andrade
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Absence of Sry in species of the vole Ellobiuspp117 - 118 Walter Just, Wolfgang Rau, Walther Vogel, Mikhail Akhverdian, Karl Fredga, Jennifer A. Marshall Graves
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Gender equality in Machado−Joseph diseasep118 Alexandra Dürr, Giovanni Stevanin, Géraldine Cancel, Nacer Abbas, Hervé Chneiweiss, Yves Agid, Josué Feingold
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Gender equality in Machado−Joseph diseasepp118 - 119 Anita L. DeStefano, Lindsay A. Farrer, Patricia Maciel, Claudia Gaspar, Guy A. Rouleau, Paula Coutinho
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Settling the myelin protein zero question in CMT1Bpp119 - 120 Laura E. Warner, Benjamin B. Roa
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A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiationpp126 - 129 Nila Patil, David R. Cox, Deepti Bhat, Malek Faham, Richard M. Myers
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A gene (PEX) with homologies to endopeptidases is mutated in patients with X−linked hypophosphatemic ricketspp130 - 136 F. Francis, S. Hennig, B. Korn, R. Reinhardt, P. de Jong, A. Poustka, H. Lehrach, P.S.N Rowe, J.N. Goulding, T. Summerfield, R. Mountford, A.P. Read, E. Popowska, E. Pronicka, K.E. Davies, J.L.H. O'Riordan, M.J. Econs, T. Nesbitt, M.K. Drezner, C. Oudet, S. Pannetier, A. Hanauer, T.M. Strom, A. Meindl, B. Lorenz, B. Cagnoli, K.L. Mohnike, J. Murken
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Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1)pp137 - 143 Jung Ahn, Hermann-Josef Lüdecke, Steffi Lindow, William A. Horton, Brendan Lee, Michael J. Wagner, Bernhard Horsthemke
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Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiencypp144 - 149 Thomas Bourgeron, Pierre Rustin, Dominique Chretien, Mark Birch-Machin, Marie Bourgeois, Evani Viegas-Péquignot, Arnold Munnich
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Quantitative locus analysis of airway hyperresponsiveness in A/J and C57BL/6J micepp150 - 154 George T. De Sanctis, Mark Merchant, David R. Beier, Robert D. Dredge, James K. Grobholz, Thomas R. Martin, Eric S. Lander
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Increased apoptosis and early embryonic lethality in mice nullizygous for the Huntington's disease gene homologuepp155 - 163 Scott Zeitlin, Jeh-Ping Liu, Deborah L. Chapman, Virginia E. Papaioannou
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A human parthenogenetic chimaerapp164 - 169 Lisa Strain, Jon P. Warner, Thomas Johnston
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Mouse models of Tay−Sachs and Sandhoff diseases differ in neurologic phenotype and ganglioside metabolismpp170 - 176 Kazunori Sango, Shoji Yamanaka, Alexander Hoffmann, Yasuharu Okuda, Alexander Grinberg, Heiner Westphal, Michael P. McDonald, Jacqueline N. Crawley, Konrad Sandhoff, Kinuko Suzuki
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A mouse model for Down syndrome exhibits learning and behaviour deficitspp177 - 184 Roger H. Reeves, Nicholas G. Irving, Timothy H. Moran, Anny Wohn, Cheryl Kitt, Sangram S. Sisodia, Cecilia Schmidt, Roderick T. Bronson
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Mice lacking ornithine−−amino−transferase have paradoxical neonatal hypoornithinaemia and retinal degenerationpp185 - 190 Tao Wang, Ann M. Lawler, Gary Steel, Ilkka Sipila, Ann H. Milam
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Long−term hepatic adenovirus−mediated gene expression in mice following CTLA4Ig administrationpp191 - 197 Mark A. Kay, Ai-Xuan Holterman, Leonard Meuse, Allen Gown, Hans D. Ochs, Peter S. Linsley
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The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individualspp198 - 200 Jeffery P. Struewing, Dvorah Abeliovich, Tamar Peretz, Naaman Avishai, Michael M. Kaback, Francis S. Collins
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A missense mutation in the neuronal nicotinic acetylcholine receptor 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsypp201 - 203 Ortrud K. Steinlein, John C. Mulley, Peter Propping, Robyn H. Wallace, Hilary A. Phillips, Grant R. Sutherland, Ingrid E. Scheffer
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Genomic imprinting of p57KIP2, a cyclin−dependent kinase inhibitor, in mousepp204 - 206 Izuho Hatada
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Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's diseasepp207 - 209 Kaoru Okuizumi, Osamu Onodera, Yoshio Namba, Kazuhiko Ikeda, Tokuo Yamamoto, Koji Seki, Akira Ueki, Shinichiro Nanko, Hajime Tanaka, Hitoshi Takahashi, Kiyomitsu Oyanagi, Hidehiro Mizusawa, Ichiro Kanazawa
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Frequency of homozygous deletion at p16/CDKN2 in primary human tumourspp210 - 212 Paul Cairns, Thomas J. Polascik, Yolanda Eby, Kaori Tokino, Joseph Califano, Adrian Merlo, Li Mao, John Herath, Robert Jenkins, William Westra, Joni L. Rutter, Alan Buckler, Edward Gabrielson, Mel Tockman, Kathleen R. Cho, Lora Hedrick, G. Steven Bova, William Isaacs, Wayne Koch, Donna Schwab
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The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21−q24pp213 - 215 Paulina Paavola, Riitta Salonen, Jean Weissenbach
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Mutations in the laminin 2−chain gene (LAMA2) cause merosin−deficient congenital muscular dystrophypp216 - 218 Anne Helbling-Leclerc, Xu Zhang, Haluk Topaloglu, Corinne Cruaud, Frédérique Tesson, Jean Weissenbach, Fernando M.S. Tomé, Ketty Schwartz, Michel Fardeau, Karl Tryggvason
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The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD familiespp219 - 222 R.F. Clark, M. Hutton, M. Fuldner, S. Froelich, E. Karran, C. Talbot, R. Crook, C. Lendon, G. Prihar, C. He, K. Korenblat, A. Martinez, M. Wragg, F. Busfield, M.I. Behrens, A. Myers, J. Norton, J. Morris, N. Mehta, C. Pearson, S. Lincoln, M. Baker, K. Duff, C. Zehr, J. Perez-Tur, H. Houlden, A. Ruiz, J. Ossa, F. Lopera, M. Arcos, L. Madrigal, J. Collinge, C. Humphreys, A. Ashworth, S. Sarner, N. Fox, R. Harvey, A. Kennedy, P. Roques, R.T. Cline, C.A. Philips, J.C. Venter, L. Forsell, K. Axelman, L. Lilius, J. Johnston, R. Cowburn, M. Viitanen, B. Winblad, K. Kosik, M. Haltia, M. Poyhonen, D. Dickson, D. Mann, D. Neary, J. Snowden, P. Lantos, L. Lannfelt, M. Rossor, G.W. Roberts, M.D. Adams, J. Hardy
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−amino−transferase have paradoxical neonatal hypoornithinaemia and retinal degeneration
4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
