Nonhomologous Robertsonian translocations form predominantly during female meiosispp231 - 232 Scott L. Page
& Lisa G. Shatter doi:10.1038/ng0397-231 References|PDF
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Telomeric transcriptional silencing in a natural contextpp232 - 233 Miguel A. Vega-Palas, Sabrina Venditti
& Ernesto Di Mauro doi:10.1038/ng0397-232 References|PDF
(400K)
Gene therapy is not eugenicsp234 John A. Wagner doi:10.1038/ng0397-234a References|PDF
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Putting a hold on 'HLA−H'p234 Bernard Merrier, Catherine Mura
& Claude Ferec doi:10.1038/ng0397-234b References|PDF
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A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Starqardt macular dystrophypp236 - 246 Rando Allikmets, Nanda Singh, Hui Sun, Noah F. Shroyer, Amy Hutchinson, Abirami Chidambaram, Bernard Gerrard, Lisa Baird, Dora Stauffer, Andy Peiffer, Amir Rattner, Philip Smallwood, Yixin Li, Kent L. Anderson, Richard Alan Lewis, Jeremy Nathans, Mark Leppert, Michael Dean
& James R. Lupski doi:10.1038/ng0397-236 Abstract + references|PDF
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Kerato-epithelin mutations in four 5q31-linked corneal dystrophiespp247 - 251 Francis L. Munier, Elena Korvatska, Assia Djemaï, Denis Le Paslier, Leonidas Zografos, Graziano Pescia
& Daniel F. Schorderet doi:10.1038/ng0397-247 Abstract + references|PDF
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The relationship between chromosome structure and function at a human telomeric regionpp252 - 257 Jonathan Flint, Karen Thomas, Gos Micklem, Helen Raynham, Kevin Clark, Norman A. Doggett, Andrew Andrew
& Douglas R. Higgs doi:10.1038/ng0397-252 Abstract + references|PDF
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Construction by gene targeting in human cells of a 'conditional' CDC2 mutant that rereplicates its DNApp258 - 265 Jane E. Itzhaki, Christopher S. Gilbert
& Andrew C.G. Porter doi:10.1038/ng0397-258 Abstract + references|PDF
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GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndromepp266 - 268 Seongman Kang, John M. Graham Jr., Ann Haskins Olney
& Leslie G. Biesecker doi:10.1038/ng0397-266 Abstract + references|PDF
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Uncoupling protein-2: a novel gene linked to obesity and hyperinsulinemiapp269 - 272 Christophe Fleury, Maria Neverova, Sheila Collins, Serge Raimbault, Odette Champigny, Corinne Levi-Meyrueis, Frederic Bouillaud, Michael F. Seldin, Richard S. Surwit, Daniel Ricquier
& Craig H. Warden doi:10.1038/ng0397-269 Abstract + references|PDF
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A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2pp273 - 276 Anthony G. Comuzzie, James E. Hixson, Laura Almasy, Braxton D. Mitchell, Michael C. Mahaney, Thomas D. Dyer, Michael P. Stern, Jean W. MacCluer
& John Blangero doi:10.1038/ng0397-273 Abstract + references|PDF
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Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31−32pp277 - 280 William C. Nichols, Daniel L. Koller, Bonnie Slovis, Tatiana Foroud, Valeri H. Terry, Nathan D. Arnold, David R. Siemieniak, Lisa Wheeler, John A. Phillips III, John H. Newman, P. Michael Conneally, David Ginsburg
& James E. Loyd doi:10.1038/ng0397-277 Abstract + references|PDF
(369K)
A mouse model for the learning and memory deficits associated with neurofibromatosis type Ipp281 - 284 Alcino J. Silva, Paul W. Frankland, Zachary Marowitz, Eugenia Friedman, George Lazlo, Dianna Cioffi, Tyler Jacks
& Roussoudan Bourtchuladze1, 4 doi:10.1038/ng0397-281 Abstract + references|PDF
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Chromosomal deletion complexes in mice by radiation of embryonic stem cellspp285 - 288 Yun You, Rebecca Bergstrom, Martina Klemm, Birgit Lederman, Heather Nelson, Christine Ticknor, Rudolf Jaenisch
& John Schimenti doi:10.1038/ng0397-285 Abstract + references|PDF
(378K)
Insulin expression in human thymus is modulated by INS VNTR alleles at the IDDM2 locuspp289 - 292 Petros Vafiadis, Simon T. Bennett, John A. Todd, Joseph Nadeau, Rosemarie Grabs, Cynthia G. Goodyer, Saman Wickramasinghe, Eleanor Colle
& Constantin Polychronakos doi:10.1038/ng0397-289 Abstract + references|PDF
(481K)
The insulin gene is transcribed in the human thymus and transcription levels correlate with allelic variation at the INS VNTR-IDDM2 susceptibility locus for type 1 diabetespp293 - 297 Alberto Pugliese, Markus Zeller, Alarico Fernandez Jr., Laura J. Zalcberg, Richard J. Bartlett, Camillo Ricordi, Massimo Pietropaolo, George S. Eisenbarth, Simon T. Bennett
& Dhavalkumar D. Patel doi:10.1038/ng0397-293 Abstract + references|PDF
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Unstable insertion in the 5' flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1pp298 - 302 Ronald G. Lafreniére, Daniel L. Rochefort, Nathalie Chrétien, Johanna M. Rommens, Jeffrey I. Cochius, Reetta Kälviäinen, Unto Nousiainen, George Patry, Kevin Farrell, Birgitta Söderfeldt, Antonio Federico, Bradford R. Hale, Otto Hernandez Cossio, Troels Sørensen, Marc A. Pouliot, Tomasz Kmiec, Peter Uldall, József Janszky, Michael R. Pranzatelli, Frederick Andermann, Eva Andermann
& Guy A. Rouleau doi:10.1038/ng0397-298 Abstract + references|PDF
(826K)
Embryonic lethality and impairment of haematopoiesis in mice heterozygous for an AML1-ETO fusion genepp303 - 306 Donald A. Yergeau, Christopher J. Hetherington, Qing Wang, Pu Zhang, Arlene H. Sharpe, Michael Binder, Miguel Marín-Padilla, Daniel G. Tenen, Nancy A. Speck
& Dong-Er Zhang doi:10.1038/ng0397-303 Abstract + references|PDF
(787K)
Heterozygous ATM mutations do not contribute to early onset of breast cancerpp307 - 310 Michael G. FitzGerald, James M. Bean, Sanjay R. Hegde, Hilal Unsal, Deborah J. MacDonald, D. Paul Harkin, Dianne M. Finkelstein, Kurt J. Isselbacher
& Daniel A. Haber doi:10.1038/ng0397-307 Abstract + references|PDF
(404K)
A non-epistatic interaction of agouti and extension in the fox, Vulpes vulpespp311 - 315 Dag Inge Våge, Dongsi Lu, Helge Klungland, Sigbjørn Lien, Stefan Adalsteinsson
& Roger D. Cone doi:10.1038/ng0397-311 Abstract + references|PDF
(836K)
Cloning, expression and chromosomal mapping of human lysosomal sialidase and characterization of mutations in sialidosispp316 - 320 Alexey V. Pshezhetsky, Catherine Richard, Lorraine Michaud, Suleiman Igdoura, Shupei Wang, Marc-André Elsliger, Jingyi Qu, Daniel Leclerc, Roy Gravel, Louis Dallaire
& Michel Potier doi:10.1038/ng0397-316 Abstract + references|PDF
(620K)
