FRAXAC2 instabilityp122 R.I. Richards, K. Holman, K. Friend, A. Staples, G.R. Sutherland, C. Oudet, V. Biancalana
& J.-L. Mandel doi:10.1038/ng0694-122a References|PDF
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FRAXAC2 instabilitypp122 - 123 E. Mornet, C. Chateau, A. Taillandier, M. Montagnon, B. Simon-Bouy, J.-L. Serre
& A. Boué doi:10.1038/ng0694-122b References|PDF
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Reply to "FRAXAC2 instability"p123 N. Zhong, C. Dobkin
& W. T. Brown doi:10.1038/ng0694-123 References|PDF
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Growing triplet repeatsp124 K. Lindblad, C. Zander, M. Schalling
& T. Hudson doi:10.1038/ng0694-124 References|PDF
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Association between atopy and variants of the subunit of the high−affinity immunoglobulin E receptorpp125 - 130 Taro Shirakawa, Airong Li, Michael Dubowitz, James W. Dekker, Ann E. Shaw, Jennie A. Faux, Chisei Ra, William O.C.M. Cookson
& Julian M. Hopkin doi:10.1038/ng0694-125 Abstract + references|PDF
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A missense mutation in the gene encoding the 1 subunit of the inhibitory glycine receptor in the spasmodic mousepp131 - 135 Stephen G. Ryan, Marion S. Buckwalter, Joseph W. Lynch, Cheryl A. Handford, Lillian Segura, Rita Shiang, John J. Wasmuth, Sally A. Camper, Peter Schofield
& Peter O'Connell doi:10.1038/ng0694-131 Abstract + references|PDF
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Glycine receptor −subunit gene mutation in spastic mouse associated with LINE−1 element insertionpp136 - 142 Stephen F. Kingsmore, Bruno Giros, David Suh, Mark Bieniarz, Marc G. Caron
& Michael F. Seldin doi:10.1038/ng0694-136 Abstract + references|PDF
(1,043K)
A new retrotransposable human L1 element from the LRE2 locus on chromosome 1q produces a chimaeric insertionpp143 - 148 Susan E. Holmes, Beth A. Dombroski, Claudia M. Krebs, Corinne D. Boehm
& Haig H. Kazazian Jr. doi:10.1038/ng0694-143 Abstract + references|PDF
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A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10pp149 - 153 Robert A. Preston, J. Christopher Post, Bronya J.B. Keats, Christopher E. Aston, Robert E. Ferrell, Janice Priest, Nassim Nouri, H. Wolfgang Losken, Colleen A. Morris, Mark R. Hurtt, John J. Mulvihill
& Garth D. Ehrlich doi:10.1038/ng0694-149 Abstract + references|PDF
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Mouse cartilage matrix deficiency (cmd) caused by a 7 bp deletion in the aggrecan genepp154 - 157 Hideto Watanabe, Koji Kimata, Sergio Line, Dave Strong, Luo-yi Gao, Christine A. Kozak
& Yoshihiko Yamada doi:10.1038/ng0694-154 Abstract + references|PDF
(424K)
Sorsby's fundus dystrophy is genetically linked to chromosome 22q13−qterpp158 - 161 Bernhard H.F. Weber, Gudrun Vogt, Werner Wolz, Elizabeth J. Ives
& Cecil C. Ewing doi:10.1038/ng0694-158 Abstract + references|PDF
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A map of the human immunoglobulin VH locus completed by analysis of the telomeric region of chromosome 14qpp162 - 168 Graham P. Cook, Ian M. Tomlinson, Gerald Walter, Harold Riethman, Nigel P. Carter, Lakjaya Buluwela, Greg Winter
& Terence H. Rabbitts doi:10.1038/ng0694-162 Abstract + references|PDF
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The origin of the major cystic fibrosis mutation (F508) in European populationspp169 - 175 N. Morral, J. Bertranpetit, X. Estivill, V. Nunes, T. Casals, J. Giménez, A. Reis, R. Varon-Mateeva, M. Macek Jr., L. Kalaydjieva, D. Angelicheva, R. Dancheva, G. Romeo, M.P. Russo, S. Garnerone, G. Restagno, M. Ferrari, C. Magnani, M. Claustres, M. Desgeorges, M. Schwartz, M. Schwarz, B. Dallapiccola, G. Novelli, C. Ferec, M. de Arce, M. Nemeti, J. Kere, M. Anvret, N. Dahl
& L. Kadasi doi:10.1038/ng0694-169 Abstract + references|PDF
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African origin of an intragenic deletion of the human P gene in tyrosinase positive oculocutaneous albinismpp176 - 179 D. Durham-Pierre, J. M. Gardner, Y. Nakatsu, R. A. King, U. Francke, A. Ching, R. Aquaron, V. del Marmol
& M. H. Brilliant doi:10.1038/ng0694-176 Abstract + references|PDF
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Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer diseasepp180 - 184 E. H. Corder, A. M. Saunders, N. J. Risch, W. J. Strittmatter, D. E. Schmechel, P. C. Gaskell Jr., J. B. Rimmler, P. A. Locke, P. M. Conneally, K. E. Schmader, G. W. Small, A. D. Roses, J. L. Haines
& M. A. Pericak-Vance doi:10.1038/ng0694-180 Abstract + references|PDF
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Familial hyperinsulinism maps to chromosome 11p14−15.1, 30 cM centromeric to the insulin genepp185 - 188 B. Glaser, K.C. Chiu, R. Anker, A. Nestorowicz, H. Landau, H. Ben-Bassat, Z. Shlomai, N. Kaiser, P.S. Thornton, C.A. Stanley, R.S. Spielman, K. Gogolin-Ewens, E. Cerasi, L. Baker, J. Rice, H. Donis-Keller
& M.A. Permutt doi:10.1038/ng0694-185 Abstract + references|PDF
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Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophypp189 - 194 Bernard C. Broughton, Herdis Steingrimsdottir, Christine A. Weber
& Alan R. Lehmann doi:10.1038/ng0694-189 Abstract + references|PDF
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Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identificationpp195 - 200 Philippe Goyette, James S. Sumner, Renate Milos, Alessandra M.V. Duncan, David S. Rosenblatt, Rowena G. Matthews
& Rima Rozen doi:10.1038/ng0694-195 Abstract + references|PDF
(899K)
Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysispp201 - 204 Esa Tahvanainen, Reijo Norio, Elvi Karila, Susanna Ranta, Jean Weissenbach, Pertti Sistonen
& Albert de la Chapelle doi:10.1038/ng0694-201 Abstract + references|PDF
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Large scale bacterial gene discovery by similarity searchpp205 - 214 Keith Robison, Walter Gilbert
& George M. Church doi:10.1038/ng0694-205 Abstract + references|PDF
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Corrigendum: Genetic dissection of autoimmune type I diabetes in the BB ratp215 doi:10.1038/ng0694-215a PDF
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Corrigendum: Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage mapp215 doi:10.1038/ng0694-215b PDF
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subunit of the high−affinity immunoglobulin E receptor
1 subunit of the inhibitory glycine receptor in the spasmodic mouse
F508) in European populations
