A dominant-negative mutation of the growth hormone receptor causes familial short staturepp13 - 14 Ruth M. Ayling, Richard Ross, Paul Towner, Sigward Von Laue, Joëlle Finidori, Soraya Moutoussamy, Charles R. Buchanan, Peter E. Clayton
& Michael R. Norman doi:10.1038/ng0597-13 References|PDF
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Intelligent linkage analysis using gene density estimatesp15 Chris F. Inglehearn doi:10.1038/ng0597-15 References|PDF
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Methylation-specif ic PCR simplifies imprinting analysispp16 - 17 Takeo Kubota, Soma Das, Susan L. Christian, Stephen B. Baylin, James G. Herman
& David H. Ledbetter doi:10.1038/ng0597-15 References|PDF
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Germline BRCA2 6174delT mutations in Ashkenazi Jewish pancreatic cancer patientspp17 - 18 Hilmi Özcelik, Beverly Schmocker, Nando Di Nicola, Xiu-Hong Shi, Bernard Langer, Malcolm Moore, Bryce R. Taylor, Steven A. Narod, Gerarda Darlington, Irene L. Andrulis, Steven Gallinger
& Mark Redston doi:10.1038/ng0597-17 References|PDF
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Genetic variation among 129 substrains and its importance for targeted mutagenesis in micepp19 - 27 Elizabeth M. Simpson, Carol C. Linder, Evelyn E. Sargent, Muriel T. Davisson, Larry E. Mobraaten
& John J. Sharp doi:10.1038/ng0597-19 Abstract + references|PDF
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Functional screening of 2 Mb of human chromosome 21q22.2 in transgenic mice implicates minibrain in learning defects associated with Down syndromepp28 - 36 Desmond J. Smith, Mary E. Stevens, Sharmila P. Sudanagunta, Roderick T. Bronson, Michael Makhinson, Ayako M. Watabe, Thomas J. O'Dell, Jingly Fung, Heinz-Ulrich G. Weier, Jan-Fang Cheng
& Edward M. Rubin doi:10.1038/ng0597-28 Abstract + references|PDF
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Many human L1 elements are capable of retrotranspositionpp37 - 43 Donna M. Sassaman, Beth A. Dombroski, John V. Moran, Michelle L. Kimberland, Thierry P. Naas, Ralph J. DeBerardinis, Abram Gabriel, Gary D. Swergold
& Haig H. Kazazian Jr doi:10.1038/ng0597-37 Abstract + references|PDF
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HIP1, a human homologue of S. cerevisiae Sla2p, interacts with membrane-associated huntingtin in the brainpp44 - 53 Michael A. Kalchman, H. Brook Koide, Krista McCutcheon, Rona K. Graham, Kerrie Nichol, Kazutoshi Nishiyama, Parsa Kazemi-Esfarjani, Francis C. Lynn, Cheryl Wellington, Martina Metzler, Y. Paul Goldberg, Ichiro Kanazawa, R. Dan. Gietz
& Michael R. Hayden doi:10.1038/ng0597-44 Abstract + references|PDF
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Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndromepp54 - 63 Ercole Rao, Birgit Weiss, Maki Fukami, Andreas Rump, Beate Niesler, Annelyse Mertz, Koji Muroya, Gerhard Binder, Stefan Kirsch, Martina Winkelmann, Gabriele Nordsiek, Udo Heinrich, Martijn H. Breuning, Michael B. Ranke, André Rosenthal, Tsutomu Ogata
& Gudrun A. Rappold doi:10.1038/ng0597-54 Abstract + references|PDF
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Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndromepp64 - 67 Danny Liaw, Debbie J. Marsh, Jing Li, Patricia L. M. Dahia, Steven I. Wang, Zimu Zheng, Shikha Bose, Katherine M. Call, Hui C. Tsou, Monica Peacoke, Charis Eng
& Ramon Parsons doi:10.1038/ng0597-64 Abstract + references|PDF
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Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomaspp68 - 73 Laura Schmidt, Fuh-Mei Duh, Fan Chen, Takeshi Kishida, Gladys Glenn, Peter Choyke, Stephen W. Scherer, Zhenping Zhuang, Irina Lubensky, Michael Dean, Rando Allikmets, Abi Chidambaram, Ulf R. Bergerheim, J. Timothy Feltis, Carme Casadevall, Agustin Zamarron, Marta Bernues, Stephane Richard, C.J.M. Lips, McClellan M. Walther, Lap-Chee Tsui, Laura Geil, Mary Lou Orcutt, Thomas Stackhouse, Jami Lipan, Leah Slife, Hiltrud Brauch, Jochen Decker, Gloria Niehans, Michael D. Hughson, Holger Moch, Stephan Storkel, Michael I. Lerman, W. Marston Linehan
& Berton Zbar doi:10.1038/ng0597-68 Abstract + references|PDF
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Chemotherapy induces transient sex chromosomal and autosomal aneuploidy in human spermpp74 - 78 Wendie A. Robbins, Marvin L. Meistrich, Dan Moore, Fredrick B. Hagemeister, Heinz-Ulrich Weier, Michael J. Cassel, Gene Wilson, Brenda Eskenazi
& Andrew J. Wyrobek doi:10.1038/ng0597-74 Abstract + references|PDF
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Organization of the Fugu rubripes Hox clusters: evidence for continuing evolution of vertebrate Hox complexespp79 - 83 Samuel Aparicio, Kelvin Hawker, Amanda Cottage, Yoshikazu Mikawa, Lin Zuo, Byrappa Venkatesh, Elson Chen, Robb Krumlauf
& Sydney Brenner doi:10.1038/ng0597-79 Abstract + references|PDF
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The parentage of a classic wine grape, Cabernet Sauvignonpp84 - 87 John E. Bowers
& Carole P. Meredith doi:10.1038/ng0597-84 Abstract + references|PDF
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Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13 in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)pp88 - 92 Gert Matthijs, Els Schollen, Els Pardon, Maria Veiga-Da-Cunha, Jaak Jaeken, Jean-Jacques Cassiman
& Emile Van Schaftingen doi:10.1038/ng0597-88 Abstract + references|PDF
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Tissue-specific selection for different mtDNA genotypes in heteroplasmic micepp93 - 95 Jack P. Jenuth, Alan C. Peterson
& Eric A. Shoubridge doi:10.1038/ng0597-93 Abstract + references|PDF
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Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeatspp96 - 99 Kersten Small, Jane Iber
& Stephen T. Warren doi:10.1038/ng0597-96 Abstract + references|PDF
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Global distribution of the CCR5 gene 32-basepair deletionpp100 - 103 Jeremy J. Martinson, Nicola H. Chapman, David C. Rees, Yan-Tat Liu
& John B Clegg doi:10.1038/ng0597-100 Abstract + references|PDF
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Academic-industry research relationships in genetics: A field apartpp104 - 108 David Blumenthal, Nancyanne Causino
& Eric G. Campbell doi:10.1038/ng0597-104 Abstract + references|PDF
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Erratum: Yeast SAS silencing genes and human genes associated with AML and HIV-1 Tat interactions are homologous with acetyltransferasesp109 doi:10.1038/ng0597-109b PDF
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-catenin — one player, two games
