A genetic linkage map of the bovine genomepp227 - 235 W. Barendse, S.M. Armitage, L.M. Kossarek, A. Shalom, B.W. Kirkpatrick, A.M. Ryan, D. Clayton, L. Li, H.L. Neibergs, N. Zhang, W.M. Grosse, J. Weiss, P. Creighton, F. McCarthy, M. Ron, A.J. Teale, R. Fries, R.A. McGraw, S.S. Moore, M. Georges, M. Soller, J.E. Womack
& D.J.S. Hetzel doi:10.1038/ng0394-227 Abstract + references|PDF
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Purification of CpG islands using a methylated DNA binding columnpp236 - 244 Sally H. Cross, Jillian A. Charlton, Xinsheng Nan
& Adrian P. Bird doi:10.1038/ng0394-236 Abstract + references|PDF
(969K)
Polymorphism of a CAG trinucleotide repeat within Sry correlates with B6.YDom sex reversalpp245 - 250 Peter Coward, Kozo Nagai, Degao Chen, Harrison D. Thomas, Claude M. Nagamine
& Yun-Fai Chris Lau doi:10.1038/ng0394-245 Abstract + references|PDF
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Altered cleavage and secretion of a recombinant −APP bearing the Swedish familial Alzheimer's disease mutationpp251 - 256 Kevin M. Felsenstein, Lisa W. Hunihan
& Susan B. Roberts doi:10.1038/ng0394-251 Abstract + references|PDF
(641K)
X−linked spastic paraplegia and Pelizaeus−Merzbacher disease are allelic disorders at the proteolipid protein locuspp257 - 262 Pascale Saugier-Veber, Arnold Munnich, Dominique Bonneau, Jean-Michel Rozet, Martine Le Merrer, Roger Gil
& Odile Boespflug-Tanguy doi:10.1038/ng0394-257 Abstract + references|PDF
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A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsiespp263 - 266 Garth A. Nicholson, Linda J. Valentijn, Annia K. Cherryson, Marina L. Kennerson, Tara L. Bragg, Robert M. DeKroon, David A. Ross, John D. Pollard, James G. Mcleod, Pieter A. Bolhuis
& Frank Baas doi:10.1038/ng0394-263 Abstract + references|PDF
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Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31−32 in three European familiespp267 - 272 B. Fontaine, J. Vale-Santos, K. Jurkat-Rott, J. Reboul, E. Plassart, C-S. Rime, A. Elbaz, R. Heine, J. Guimarães, J. Weissenbach, N. Baumann, M. Fardeau
& F. Lehmann-Horn doi:10.1038/ng0394-267 Abstract + references|PDF
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Genomic instability in repeated sequences is an early somatic event in colorectal tumorigenesis that persists after transformationpp273 - 281 Darryl Shibata, Miguel Angel Peinado, Yurij lonov, Sergei Malkhosyan
& Manuel Perucho doi:10.1038/ng0394-273 Abstract + references|PDF
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A complex bilateral polysyndactyly disease locus maps to chromosome 7q36pp282 - 286 Olga Tsukurov, Annemie Boehmer, Jack Flynn, Jean-Philippe Nicolai, Ben C. J. Hamel, Saskia Traill, David Zaleske, Henry J. Mankin, Howard Yeon, Chrystal Ho, Cliff Tabin, J. G. Seidman
& Christine Seidman doi:10.1038/ng0394-282 Abstract + references|PDF
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The gene for triphalangeal thumb maps to the subtelomeric region of chromosome 7qpp287 - 292 Peter Heutink, Julia Zguricas, Linda van Oosterhout, Guido J. Breedveld, Leon Testers, Lodewijk A. Sandkuijl, Pieter J.L.M. Snijders, Jean Weissenbach, Dick Lindhout, Steven E.R Hovius
& Ben A. Oostra doi:10.1038/ng0394-287 Abstract + references|PDF
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Mutations in the 2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosapp293 - 298 Leena Pulkkinen, Angela M. Christiano, Tomi Airenne, Heli Haakana, Karl Tryggvason
& Jouni Uitto doi:10.1038/ng0394-293 Abstract + references|PDF
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Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the 2 subunit of nicein/kalinin (LAMININ−5)pp299 - 304 Daniel Aberdam, Marie-Florence Galliano, Joëlle Vailly, Leena Pulkkinen, Jeannette Bonifas, Angela M. Christiano, Karl Tryggvason, Jouni Uitto, Ervin H. Epstein Jr, Jean-Paul Ortonne
& Guerrino Meneguzzi doi:10.1038/ng0394-299 Abstract + references|PDF
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Mosaic and polymorphic imprinting of the WT1 gene in humanspp305 - 309 Yoshihiro Jinno, Kankatsu Yun, Kunihiko Nishiwaki, Takeo Kubota, Osamu Ogawa, Anthony E. Reeve
& Norio Niikawa doi:10.1038/ng0394-305 Abstract + references|PDF
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Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprintingpp310 - 313 Stephen J. Giddings, Christopher D. King, Kristen W. Harman, James F. Flood
& Lynn R. Carnaghi doi:10.1038/ng0394-310 Abstract + references|PDF
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The gene for achondroplasia maps to the telomeric region of chromosome 4ppp314 - 317 Milen Velinov, Susan A. Slaugenhaupt, Ivaylo Stoilov, Charles I. Scott Jr., James F. Gusella
& Petros Tsipouras doi:10.1038/ng0394-314 Abstract + references|PDF
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A gene for achondroplasia−hypochondroplasia maps to chromosome 4ppp318 - 321 Martine Le Merrer, Francis Rousseau, Laurence Legeai-Mallet, Jean-Christophe Landais, Anna Pelet, Jacky Bonaventure, Marek Sanak, Jean Weissenbach, Claude Stoll, Arnold Munnich
& Pierre Maroteaux doi:10.1038/ng0394-318 Abstract + references|PDF
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−APP bearing the Swedish familial Alzheimer's disease mutation
2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosa
