Carboxy-terminally truncated Gli3 proteins associate with Smadspp325 - 326 Fang Liu, Joan Massagué
& Ariel Ruiz i Altaba. doi:10.1038/3793 Full text|PDF
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MSH2 genomic deletions are a frequent cause of HNPCCpp326 - 328 Juul Wijnen, Heleen van der Klift, Hans Vasen, P. Meera Khan, Fred Menko, Carli Tops, Hanne Meijers Heijboer, Dick Lindhout, Pål Møller
& Ricardo Fodde. doi:10.1038/3795 Full text|PDF
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Allelic variation in ABCR associated with Stargardt
disease but not age-related macular degenerationpp328 - 329 Edwin M. Stone., Andrew R. Webster, Kimberlie Vandenburgh, Luan M. Streb, Robin R. Hockey, Andrew J. Lotery
& Val C. Sheffield doi:10.1038/3798 Full text|PDF
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Genetics without frontierspp329 - 330 Newton E. Morton doi:10.1038/3801 Full text|PDF
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Reply to Genetics without frontierspp330 - 331 Julia White, Hester Wain, Elspeth Bruford
& Sue Povey. doi:10.1038/3802 Full text|PDF
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The Human Genome Project after a decade: policy issuespp333 - 335 John Burris, Robert Cook-Deegan
& Bruce Alberts doi:10.1038/3803 Abstract|Full text|PDF
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SURF1, encoding a factor involved in the biogenesis of cytochrome
c oxidase, is mutated in Leigh syndromepp337 - 343 Zhiqing Zhu, Jianbo Yao, Timothy Johns, Katherine Fu, Isabelle De Bie, Carol Macmillan, Andrew P. Cuthbert, Robert F. Newbold, Jia-chi Wang, Mario Chevrette, Garry K. Brown, Ruth M. Brown
& Eric A. Shoubridge. doi:10.1038/3804 Abstract|Full text|PDF
(424K)
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Rpe65 is necessary for production of 11-cis-vitamin A in
the retinal visual cyclepp344 - 351 T. Michael Redmond., Shirley Yu, Eric Lee, Dean Bok, Duco Hamasaki, Ning Chen, Patrice Goletz, Jian-Xing Ma, Rosalie K. Crouch
& Karl Pfeifer doi:10.1038/3813 Abstract|Full text|PDF
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A homeobox gene, HLXB9, is the major locus for dominantly inherited
sacral agenesispp358 - 361 Alison J. Ross, Victor Ruiz-Perez, Yiming Wang, Donna-Marie Hagan, Steve Scherer, Sally A. Lynch, Susan Lindsay, Emily Custard, Elena Belloni, David I. Wilson, Roy Wadey, Frances Goodman, Karen Helene Orstavik, Tom Monclair, Steve Robson, William Reardon, John Burn, Pete Scambler
& Tom Strachan. doi:10.1038/3828 Abstract|Full text|PDF
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Genomic imprinting is disrupted in interspecific Peromyscus hybrids
pp362 - 365 Paul B. Vrana, Xiao-Juan Guan, Robert S. Ingram
& Shirley M. Tilghman. doi:10.1038/3833 Abstract|Full text|PDF
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Mutations in the human connexin gene GJB3 cause erythrokeratodermia
variabilispp366 - 369 Gabriele Richard, Lisa E. Smith, Regina A. Bailey, Peter Itin, Daniel Hohl, Ervin H. Epstein Jr, John J. DiGiovanna, John G. Compton
& Sherri J. Bale. doi:10.1038/3840 Abstract|Full text|PDF
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Mutations in the gene encoding gap junction protein -3 associated
with autosomal dominant hearing impairmentpp370 - 373 Jia-hui Xia., Chun-yu Liu, Bei-sha Tang, Qian Pan, Lei Huang, He-ping Dai, Bao-rong Zhang, Wei Xie, Dong-xu Hu, Duo Zheng, Xiao-liu Shi, De-an Wang, Kun Xia, Kuan-ping Yu, Xiao-dong Liao, Yong Feng, Yi-feng Yang, Jian-yun Xiao, Ding-hua Xie
& Jian-zheng Huang doi:10.1038/3845 Abstract|Full text|PDF
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The winged helix transcription factor Fkh10 is required for normal development
of the inner earpp374 - 376 Malin Hulander, Wolfgang Wurst, Peter Carlsson
& Sven Enerbäck. doi:10.1038/3850 Abstract|Full text|PDF
(183K)
Cyclin A1 is required for meiosis in the male mousepp377 - 380 Dong Liu, Martin M. Matzuk, Weng Kong Sung, Qiuxia Guo, Pei Wang
& Debra J. Wolgemuth. doi:10.1038/3855 Abstract|Full text|PDF
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Engineering chromosomes in mice through targeted meiotic recombination
(TAMERE)pp381 - 384 Yann Hérault, Minoo Rassoulzadegan, François Cuzin
& Denis Duboule. doi:10.1038/3861 Abstract|Full text|PDF
(402K)
Alleles of APC modulate the frequency and classes of mutations
that lead to colon polypspp385 - 388 Lisa N. Spirio, Wade Samowitz, Jennifer Robertson, Margaret Robertson, Randall W. Burt, Mark Leppert
& Ray White. doi:10.1038/3865 Abstract|Full text|PDF
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Tetracycline-regulatable factors with distinct dimerization domains allow
reversible growth inhibition by p16pp389 - 393 Fabio M.V. Rossi, Oivin M. Guicherit, Albert Spicher, Andrew M. Kringstein, Karoly Fatyol, Bruce T. Blakely
& Helen M. Blau. doi:10.1038/3871 Abstract|Full text|PDF
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Defective IL7R expression in T-B+NK
+ severe combined immunodeficiencypp394 - 397 Anne Puel, Steven F. Ziegler, Rebecca H. Buckley
& Warren J. Leonard. doi:10.1038/3877 Abstract|Full text|PDF
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ATM associates with and phosphorylates p53: mapping the region of interaction
pp398 - 400 Kum Kum Khanna., Katherine E. Keating, Sergei Kozlov, Shaun Scott, Magtouf Gatei, Karen Hobson, Yoichi Taya, Brian Gabrielli, Doug Chan, Susan P. Lees-Miller
& Martin F. Lavin doi:10.1038/3882 Abstract|Full text|PDF
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Genetic control of arthritis onset, severity and chronicity in a model
for rheumatoid arthritis in ratspp401 - 404 Carina Vingsbo-Lundberg, Niklas Nordquist, Peter Olofsson, Mats Sundvall, Tore Saxne, Ulf Pettersson
& Rikard Holmdahl. doi:10.1038/3887 Abstract|Full text|PDF
(143K)
-3 associated
with autosomal dominant hearing impairment
