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A small step for gene therapy pp323 - 324
doi:10.1038/ng0494-323
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(282K)
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| News and Views | Top |
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Heroic gene surgery pp325 - 326
David Weatherall
doi:10.1038/ng0494-325
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(231K)
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Computing the genetic map pp326 - 328
G. Mark Lathrop
doi:10.1038/ng0494-326
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(481K)
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Cystinuria defect expresses itself pp328 - 329
Ernest M. Wright
doi:10.1038/ng0494-328
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(225K)
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Craniofacial malformations: towards a molecular understanding pp329 - 330
Mark W. J. Ferguson
doi:10.1038/ng0494-329
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(213K)
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| Correspondence | Top |
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Unequal expression of NF1 alleles p331
Sven Hoffmeyer, Günter Assum, Dieter Kaufmann
& Winfrid Krone
doi:10.1038/ng0494-331
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(135K)
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Altered imprinting in lung cancer pp332 - 333
Hiroko Suzuki, Ryuzo Ueda, Toshitada Takahashi
& Takashi Takahashi
doi:10.1038/ng0494-332
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(267K)
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Proteolipid protein gene dosage effect in Pelizaeus−Merzbacher disease pp333 - 334
David Ellis
& Sue Malcolm
doi:10.1038/ng0494-333
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(229K)
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Chromosome 4p16 and osteochondroplasias p334
Miguel Urioste, Maria Luisa Martinez-Frias, Eva Bermejo, Amelia Villa, Nicolas Jimenez, Dolores Romero
& Carmen Nieto
doi:10.1038/ng0494-334
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(115K)
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| Articles | Top |
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Successful ex vivo gene therapy directed to liver in a patient with familial hypercholesterolaemia pp335 - 341
Mariann Grossman, Steven E. Raper, Karen Kozarsky, Evan A. Stein, John F. Engelhardt, David Muller, Paul J. Lupien
& James M. Wilson
doi:10.1038/ng0494-335
Abstract + references | PDF
(1,006K)
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Comparative chromosome painting discloses homologous segments in distantly related mammals pp342 - 347
Harry Scherthan, Thomas Cremer, Ulfur Arnason, Heinz-Ulrich Weier, Antonio Lima-de-Faria
& Lutz Frönicke
doi:10.1038/ng0494-342
Abstract + references | PDF
(767K)
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Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development pp348 - 356
Ichiro Satokata
& Richard Maas
doi:10.1038/ng0494-348
Abstract + references | PDF
(1,344K)
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Multifactorial inheritance of neural tube defects: localization of the major gene and recognition of modifiers in ct mutant mice pp357 - 362
Paul E. Neumann, Wayne N. Frankel, Verity A. Letts, John M. Coffin, Andrew J. Copp
& Merton Bernfield
doi:10.1038/ng0494-357
Abstract + references | PDF
(651K)
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A mutation in the Ter gene causing increased susceptibility to testicular teratomas maps to mouse chromosome 18 pp363 - 368
Yoshinobu Asada, Don S. Varnum, Wayne N. Frankel
& Joseph H. Nadeau
doi:10.1038/ng0494-363
Abstract + references | PDF
(603K)
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The mottled gene is the mouse homologue of the Menkes disease gene pp369 - 373
Barbara Levinson, Christopher Vulpe, Bruce Elder, Christopher Martin, Frank Verley, Seymour Packman
& Jane Gitschier
doi:10.1038/ng0494-369
Abstract + references | PDF
(784K)
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Mutations in the murine homologue of the Menkes gene in dappled and blotchy mice pp374 - 378
Julian F.B. Mercer, Andrew Grimes, Loreta Ambrosini, Paul Lockhart, Jennifer A. Paynter, Herman Dierick
& Thomas W. Glover
doi:10.1038/ng0494-374
Abstract + references | PDF
(838K)
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Long−range mapping of gaps and telomeres with RecA−assisted restriction endonuclease (RARE) cleavage pp379 - 383
Lance J. Ferrin
& R. Daniel Camerini-Otero
doi:10.1038/ng0494-379
Abstract + references | PDF
(581K)
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Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map pp384 - 390
Tara Cox Matise, Mark Perlin
& Aravinda Chakravarti
doi:10.1038/ng0494-384
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(760K)
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Integrated human genome−wide maps constructed using the CEPH reference panel pp391 - 393
Kenneth H. Buetow, James L. Weber, Susan Ludwigsen, Titia Scherpbier-Heddema, Geoffrey M. Duyk, Val C. Sheffield, Zhenyuan Wang
& Jeffrey C. Murray
doi:10.1038/ng0494-391
Abstract + references | PDF
(290K)
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Cloning of PBDX, an MIC2-related gene that spans the pseudoautosomal boundary on chromosome Xp pp394 - 400
Nathan A. Ellis, Tian-Zhang Ye, Susan Patton, James German, Peter N. Goodfellow
& Polly Weller
doi:10.1038/ng0494-394
Abstract + references | PDF
(690K)
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Holt−Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12q pp401 - 404
Jonathan A. Terrett, Ruth Newbury-Ecob, Gareth S. Cross, Iain Fenton, J. Alexander Raeburn, Ian D. Young
& J. David Brook
doi:10.1038/ng0494-401
Abstract + references | PDF
(363K)
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A gene for Holt−Oram syndrome maps to the distal long arm of chromosome 12 pp405 - 408
Damien Bonnet, Anna Pelet, Laurence Legeai-Mallet, Daniel Sidi, Michèle Mathieu, Philippe Parent, Henri Plauchu, Françoise Serville, Albert Schinzel, Jean Weissenbach, Jean Kachaner, Arnold Munnich
& Stanislas Lyonnet
doi:10.1038/ng0494-405
Abstract + references | PDF
(399K)
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Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm pp409 - 414
Håkan Telenius, Berry Kremer, Y. Paul Goldberg, Jane Theilmann, Susan E. Andrew, Jutta Zeisler, Shelin Adam, Cheryl Greenberg, Elizabeth J. Ives, Lorne A. Clarke
& Michael R. Hayden
doi:10.1038/ng0494-409
Abstract + references | PDF
(719K)
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Localization of a gene causing cystinuria to chromosome 2p pp415 - 419
Elon Pras, Nadir Arber, Ivona Aksentijevich, Giora Katz, Jonathan M. Schapiro, Leandrea Prosen, Luis Gruberg, Daniela Harel, Uri Liberman, Jean Weissenbach, Mordechai Pras
& Daniel L. Kastner
doi:10.1038/ng0494-415
Abstract + references | PDF
(423K)
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Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystine pp420 - 425
María Julia Calonge, Paolo Gasparini, Josep Chillarón, Miguel Chillón, Michele Gallucci, Ferran Rousaud, Leopoldo Zelante, Xavier Testar, Bruno Dallapiccola, Franco Di Silverio, Pedro Barceló, Xavier Estivill, Antonio Zorzano, Virginia Nunes
& Manuel Palacín
doi:10.1038/ng0494-420
Abstract + references | PDF
(692K)
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Ceruloplasmin gene defect associated with epilepsy in EL mice pp426 - 431
Caroline E. Garey, Alexander L. Schwarzman, Matthew L. Rise
& Thomas N. Seyfried
doi:10.1038/ng0494-426
Abstract + references | PDF
(592K)
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