Transgenic mice containing a human heavy chain immunoglobulin gene fragment cloned in a yeast artificial chromosomepp117 - 123 Ted K. Choi, Paul W. Hollenbach, Barbara E. Pearson, Roanna M. Ueda, Gregory N. Weddell, Carole G. Kurahara, Clive S. Woodhouse, Robert M. Kay
& Jeanne F. Loring doi:10.1038/ng0693-117 Abstract + references|PDF
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Motheaten and viable motheaten mice have mutations in the haematopoietic cell phosphatase genepp124 - 129 Hing Wo Tsui, Katherine A. Siminovitch, Loretta de Souza
& Florence W.L. Tsui doi:10.1038/ng0693-124 Abstract + references|PDF
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Recessive mutations in the gene encoding the −subunit of rod phosphodiesterase in patients with retinitis pigmentosapp130 - 134 Margaret E. McLaughlin, Michael A. Sandberg, Eliot L. Berson
& Thaddeus P. Dryja doi:10.1038/ng0693-130 Abstract + references|PDF
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Direct detection of novel expanded trinucleotide repeats in the human genomepp135 - 139 Martin Schalling, Thomas J. Hudson, Kenneth H. Buetow
& David E. Housman doi:10.1038/ng0693-135 Abstract + references|PDF
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Mitotic stability of fragile X mutations in differentiated cells indicates early post−conceptional trinucleotide repeat expansionpp140 - 142 Doris Wöhrle, Ingeborg Hennig, Walther Vogel
& Peter Steinbach doi:10.1038/ng0693-140 Abstract + references|PDF
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The full mutation in the FMR−1 gene of male fragile X patients is absent in their spermpp143 - 146 Edwin Reyniers, Lieve Vits, Kristel De Boulle, Bernadette Van Roy, Desirée Van Velzen, Esther de Graaff, Annemieke J.M.H. Verkerk, Hugo Z.J. Jorens, John K. Darby, Ben Oostra
& Patrick J. Willems doi:10.1038/ng0693-143 Abstract + references|PDF
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Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brainpp147 - 153 Marc Abitbol, Christian Menini, Anne-Lise Delezoide, Thomas Rhyner, Michel Vekemans
& Jacques Mallet doi:10.1038/ng0693-147 Abstract + references|PDF
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Correction of lysosomal storage in the liver and spleen of MPS VII mice by implantation of genetically modified skin fibroblastspp154 - 159 Philippe Moullier, Delphine Bohl, Jean-Michel Heard
& Olivier Danos doi:10.1038/ng0693-154 Abstract + references|PDF
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Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosispp160 - 164 Anat Blumenfeld, Susan A. Slaugenhaupt, Felicia B. Axelrod, Diane E. Lucente, Channa Maayan, Christopher B. Liebert, Laurie J. Ozelius, James A. Trofatter, Jonathan L. Haines, Xandra O. Breakefield
& James F. Gusella doi:10.1038/ng0693-160 Abstract + references|PDF
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Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination eventspp165 - 169 B. Weiffenbach, J. Dubois, D. Storvick, R. Tawil, S.J. Jacobsen, J. Gilbert, C. Wijmenga, J.R. Mendell, S. Winokur, M.R. Altherr, P. Schultz, S. Olandt, R.R. Frants, M. Pericak-Vance
& R.C. Griggs doi:10.1038/ng0693-165 Abstract + references|PDF
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Assignment of an autosomal sex reversa− locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3−q25.1pp170 - 174 N. Tommerup, W. Schempp, P. Meinecke, S. Pedersen, L. Bolund, C. Brandt, C. Goodpasture, P. Guldberg, K.R. Held, H. Reinwein, O.D. Saugstad, G. Scherer, O. Skjeldal, R. Toder, J. Westvik, C.B. van der Hagen
& U. Wolf doi:10.1038/ng0693-170 Abstract + references|PDF
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Fusion of the dominant negative transcription regulator CHOP with a novel gene FUS by translocation t(12;16) in malignant liposarcomapp175 - 180 T.H. Rabbitts, A. Forster, R. Larson
& P. Nathan doi:10.1038/ng0693-175 Abstract + references|PDF
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A cosmid contig and high resolution restriction map of the 2 megabase region containing the Huntington's disease genepp181 - 186 Sarah Baxendale, Marcy E. MacDonald, Richard Mott, Fiona Francis, Carol Lin, Susan F. Kirby, Marianne James, Günther Zehetner, Holger Hummerich, John Valdes, Francis S. Collins, Larry J. Deaven, James F. Gusella, Hans Lehrach
& Gillian P. Bates doi:10.1038/ng0693-181 Abstract + references|PDF
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Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N−myc amplificationpp187 - 190 Huib Caron, Peter van Sluis, Melanie van Hoeve, Jan de Kraker, Johannes Bras, Rosalyn Slater, Marcel Mannens, P.A. Voûte, Andries Westerveld
& Rogier Versteeg doi:10.1038/ng0693-187 Abstract + references|PDF
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Preferential amplification of the paternal allele of the N−myc gene in human neuroblastomaspp191 - 194 Judy M. Cheng, Jill L. Hiemstra, Sandra S. Schneider, Anna Naumova, Nai-Kong V. Cheung, Susan L. Cohn, Lisa Diller, Carmen Sapienza
& Garrett M. Brodeur doi:10.1038/ng0693-191 Abstract + references|PDF
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Drosophila awdK−pn, a homologue of the metastasis suppressor gene nm23, suppresses the Tum−I haematopoietic oncogenepp195 - 201 Dawn L. Zinyk, Bethany G. McGonnigal
& Charles R. Dearolf doi:10.1038/ng0693-195 Abstract + references|PDF
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A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jewspp202 - 205 Michael A. Whitney, Hiroshi Saito, Petra M. Jakobs, Rachel A. Gibson, Robb E. Moses
& Markus Grompe doi:10.1038/ng0693-202 Abstract + references|PDF
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Microsatellite mapping of a gene affecting horn development in Bos tauruspp206 - 210 Michel Georges, Roger Drinkwater, Tracey King, Anuradha Mishra, Stephen S. Moore, Dahlia Nielsen, Leslie S. Sargeant, Anita Sorensen, Michael R. Steele, Xuyun Zhao, James E. Womack
& Jay Hetzel doi:10.1038/ng0693-206 Abstract + references|PDF
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−subunit of rod phosphodiesterase in patients with retinitis pigmentosa
