Genetic dissection of complex traitspp355 - 356 John S. Witte, Robert C. Elston
& Nicholas J. Schork doi:10.1038/ng0496-355 References|PDF
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Genetic dissection of complex traitspp356 - 357 David Curtis doi:10.1038/ng0496-356 References|PDF
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Genetic dissection of complex traitspp357 - 358 Eric Lander Leonid Kruglyak doi:10.1038/ng0496-357 References|PDF
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XNP mutation in a large family with Juberg-Marsidi syndromepp359 - 360 Laurent Villard, Josef Gecz, Jean François Mattéi, Michel Fontés, Pascale Saugier-Veber, Arnold Munnich
& Stanislas Lyonnet doi:10.1038/ng0496-359 References|PDF
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Reconstructing the ancient mariners of humanspp360 - 361 Hugh M. Robertson, Karen L. Zumpano, Allan R. Lohe
& Daniel L. Hartl doi:10.1038/ng0496-360 References|PDF
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The most beautiful peoplepp361 - 362 Hilton Stowell doi:10.1038/ng0496-361 References|PDF
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Karyotyping human chromosomes by combinatorial multi-fluor FISHpp368 - 375 Michael R. Speicher, Stephen Gwyn Ballard
& David C. Ward doi:10.1038/ng0496-368 Abstract + references|PDF
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Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiationpp376 - 384 Margit Burmeister, Jakub Novak, Mei-Ying Liang, Sharmila Basu, Lynda Ploder, Norman L. Hawes, Danka Vidgen, Frank Hoover, Daniel Goldman, Vitauts I. Kalnins, Thomas H. Roderick, Benjamin A. Taylor, Mark H. Hankin
& Roderick R. Mclnnes doi:10.1038/ng0496-376 Abstract + references|PDF
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A novel X-linked gene, G4.5. is responsible for Barth syndromepp385 - 389 Silvia Bione, Patrizia D'Adamo, Elena Maestrini, Agi K. Gedeon, Pieter A. Bolhuis
& Daniela Toniolo doi:10.1038/ng0496-385 Abstract + references|PDF
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Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3pp390 - 397 Jennifer S. Colvin, Barbara A. Bohne, Gary W. Harding, Donald G. McEwen
& David M. Ornitz doi:10.1038/ng0496-390 Abstract + references|PDF
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An X-chromosome linked locus contributes to abnormal placental development in mouse interspecific hybridspp398 - 403 Ulrich Zechner, Matthias Reule, Annie Orth, François Bonhomme, Bärbel Strack, Jean-Louis Guénet, Horst Hameister
& Reinald Fundele doi:10.1038/ng0496-398 Abstract + references|PDF
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Mouse Dax1 expression is consistent with a role in sex determination as well as in adrenal and hypothalamus functionpp404 - 409 Amanda Swain, Elena Zanaria, Adam Hacker, Robin Lovell-Badge
& Giovanna Camerino doi:10.1038/ng0496-404 Abstract + references|PDF
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A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuriapp410 - 416 J. Andrew Keightley, Kristen C. Hoffbuhr, Miriam D. Burton, Virginia M. Salas, Wendy S.W. Johnston, Andrew M.W. Penn, Neil R.M. Buist
& Nancy G. Kennaway doi:10.1038/ng0496-410 Abstract + references|PDF
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Mitochondrial DNA sequence heteroplasmy in the Grand Duke of Russia Georgij Romanov establishes the authenticity of the remains of Tsar Nicholas IIpp417 - 420 Pavel L. Ivanov, Mark J. Wadhams, Rhonda K. Roby, Mitchell M. Holland, Victor W. Weedn
& Thomas J. Parsons doi:10.1038/ng0496-417 Abstract + references|PDF
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Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4pp421 - 423 Beth Coyle, Rebecca Coffey, John A.L. Armour, Eleanor Gausden, Ze'ev Hochberg, Ashley Grossman, Keith Britton, Marcus Pembrey, William Reardon
& Richard Trembath doi:10.1038/ng0496-421 Abstract + references|PDF
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Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organificationpp424 - 426 Val C. Sheffield, Zaki Kraiem, John C. Beck, Darryl Nishimura, Edwin M. Stone, Muhamad Salameh, Orit Sadeh
& Benjamin Glaser doi:10.1038/ng0496-424 Abstract + references|PDF
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A locus for bipolar affective disorder on chromosome 4ppp427 - 430 Douglas H.R. Blackwood, Lin He, Stewart W. Morris, Alan McLean, Claire Whitton, Marian Thomson, Maura T. Walker, Kirstie Woodburn, Cliff M. Sharp, Allan F. Wright,, Yoshiro Shibasaki, David M. St. Clair, David J. Poreous
& Walter J. Muir doi:10.1038/ng0496-427 Abstract + references|PDF
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A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amishpp431 - 435 Edward I. Ginns, Jurg Ott, Janice A. Egeland, Cleona R. Allen, Cathy S.J. Fann, David L. Pauls, Jean Weissenbach, John P. Carulli, Kathleen M. Falls, Tim P. Keith
& Steven M. Paul doi:10.1038/ng0496-431 Abstract + references|PDF
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Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23pp436 - 441 Nelson B. Freimer, Victor I. Reus, Michael A. Escamilla, L. Alison Mclnnes, Mitzi Spesny, Pedro Leon, Susan K. Service, Lauren B. Smith, Sandra Silva, Eugenia Rojas, Alvaro Gallegos, Luis Meza, Eduardo Fournier, Siamak Baharloo, Kathleen Blankenship, David J. Tyler, Steven Batki, Sophia Vinogradov, Jean Weissenbach, Samuel H. Barondes
& Lodewijk A. Sandkuijl doi:10.1038/ng0496-436 Abstract + references|PDF
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Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)pp442 - 444 Patrick Edery, Tania Attie, Jeanne Amiel, Anna Pelet, Charis Eng, Robert M.W. Hofstra, Helene Martelli, Christelle Bidaud, Arnold Munnich
& Stanislas Lyonnet doi:10.1038/ng0496-442 Abstract + references|PDF
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A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)pp445 - 447 Robert M.W. Hofstra, Jan Osinga, Gita Tan-Sindhunata, Ying Wu, Erik-J. Kamsteeg, Rein P. Stulp, Conny van Ravenswaaij-Arts, Daniëlle Majoor-Krakauer, Misha Angrist, Aravinda Chakravarti, Carel Meijers
& Charles H.C.M. Buys doi:10.1038/ng0496-445 Abstract + references|PDF
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Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemiapp448 - 451 Ming Chen, Darrell J. Tomkins, Wojtek Auerbach, Colin McKerlie, Hagop Youssoufian, Lili Liu, Olga Gan, Madeleine Carreau, Anna Auerbach, Tim Groves, Cynthia J. Guidos, Melvin H. Freedman, Jay Cross, Dean H. Percy, John E. Dick, Alexandra L. Joyner
& Manuel Buchwald doi:10.1038/ng0496-448 Abstract + references|PDF
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Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpointpp452 - 454 Astrid Schulze, Claus Hansen, Niels Erik Skakkebæk, Karen Brøndum-Nielsen, David H. Ledbetter
& Niels Tommerup doi:10.1038/ng0496-452 Abstract + references|PDF
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Genetic mapping of a pulmonary adenoma resistance locus (Par1) in mousepp455 - 457 Giacomo Manenti, Manuela Gariboldi, Ramu Elango, Antonio Fiorino, Laura De Gregorio, F. Stefania Falvella, Kent Hunter, David Housman, Marco A. Pierotti
& Tommaso A. Dragani doi:10.1038/ng0496-455 Abstract + references|PDF
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Erratum: Hepatocytes corrected by gene therapy are selected in vivo in a murine model of hereditary tyrosinaemia type Ip458 doi:10.1038/ng0496-458a PDF
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Erratum: Human choroideremia protein contains a FAD-binding domainp458 doi:10.1038/ng0496-458b PDF
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Corrigendum: Loss of NF1 results in activation of the Ras signaling pathway and leads to aberrant growth in haematopoietic cellsp458 doi:10.1038/ng0496-458c PDF
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