Proteolipid protein gene dosage effect in Pelizaeus−Merzbacher diseasepp333 - 334 David Ellis
& Sue Malcolm doi:10.1038/ng0494-333 References|PDF
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Chromosome 4p16 and osteochondroplasiasp334 Miguel Urioste, Maria Luisa Martinez-Frias, Eva Bermejo, Amelia Villa, Nicolas Jimenez, Dolores Romero
& Carmen Nieto doi:10.1038/ng0494-334 References|PDF
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Successful ex vivo gene therapy directed to liver in a patient with familial hypercholesterolaemiapp335 - 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
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Comparative chromosome painting discloses homologous segments in distantly related mammalspp342 - 347 Harry Scherthan, Thomas Cremer, Ulfur Arnason, Heinz-Ulrich Weier, Antonio Lima-de-Faria
& Lutz Frönicke doi:10.1038/ng0494-342 Abstract + references|PDF
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Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth developmentpp348 - 356 Ichiro Satokata
& Richard Maas doi:10.1038/ng0494-348 Abstract + references|PDF
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Multifactorial inheritance of neural tube defects: localization of the major gene and recognition of modifiers in ct mutant micepp357 - 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
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A mutation in the Ter gene causing increased susceptibility to testicular teratomas maps to mouse chromosome 18pp363 - 368 Yoshinobu Asada, Don S. Varnum, Wayne N. Frankel
& Joseph H. Nadeau doi:10.1038/ng0494-363 Abstract + references|PDF
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The mottled gene is the mouse homologue of the Menkes disease genepp369 - 373 Barbara Levinson, Christopher Vulpe, Bruce Elder, Christopher Martin, Frank Verley, Seymour Packman
& Jane Gitschier doi:10.1038/ng0494-369 Abstract + references|PDF
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Mutations in the murine homologue of the Menkes gene in dappled and blotchy micepp374 - 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
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Long−range mapping of gaps and telomeres with RecA−assisted restriction endonuclease (RARE) cleavagepp379 - 383 Lance J. Ferrin
& R. Daniel Camerini-Otero doi:10.1038/ng0494-379 Abstract + references|PDF
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Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage mappp384 - 390 Tara Cox Matise, Mark Perlin
& Aravinda Chakravarti doi:10.1038/ng0494-384 Abstract + references|PDF
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Integrated human genome−wide maps constructed using the CEPH reference panelpp391 - 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
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Cloning of PBDX, an MIC2-related gene that spans the pseudoautosomal boundary on chromosome Xppp394 - 400 Nathan A. Ellis, Tian-Zhang Ye, Susan Patton, James German, Peter N. Goodfellow
& Polly Weller doi:10.1038/ng0494-394 Abstract + references|PDF
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Holt−Oram syndrome is a genetically heterogeneous disease with one locus mapping to human chromosome 12qpp401 - 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
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A gene for Holt−Oram syndrome maps to the distal long arm of chromosome 12pp405 - 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
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Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and spermpp409 - 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
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Localization of a gene causing cystinuria to chromosome 2ppp415 - 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
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Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystinepp420 - 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
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Ceruloplasmin gene defect associated with epilepsy in EL micepp426 - 431 Caroline E. Garey, Alexander L. Schwarzman, Matthew L. Rise
& Thomas N. Seyfried doi:10.1038/ng0494-426 Abstract + references|PDF
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