Missense rhodopsin mutation in a family with recessive RPpp10 - 11 Govindasamy Kumaramanickavel, Marion Maw, Michael J. Denton, Sheila John, C.R.Srisailapathy Srikumari, Ulrike Orth, Ralph Oehlmann
& Andreas Gal doi:10.1038/ng0994-10 References|PDF
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Reply to "RFLVs in mottled dappled alleles"p12 B. Levinson, C. Vulpe, B. Elder, C. Martin, S. Packman, J. Gitschier
& F. Verly doi:10.1038/ng0994-12 References|PDF
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Parental origin of WT1 mutations and mental retardation in WAGR syndromep13 Vicki Huff doi:10.1038/ng0994-13a References|PDF
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Reply to "Parental origin of WT1 mutations and mental retardation in WAGR syndrome"pp13 - 14 Yoshihiro Jinno
& Anthony Reeve doi:10.1038/ng0994-13b References|PDF
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Germline p16 mutations in familial melanomapp15 - 21 Christopher J. Hussussian, Jeffery P. Struewing, Alisa M. Goldstein, Paul A. T. Higgins, Delphine S. Ally, Michelle D. Sheahan, Wallace H. Clark Jr., Margaret A. Tucker
& Nicholas C. Dracopoli doi:10.1038/ng0994-15 Abstract + references|PDF
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Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locuspp22 - 26 A. Kamb, D. Shattuck-Eidens, R. Eeles, Q. Liu, N. A. Gruis, W. Ding, C. Hussey, T. Tran, Y. Miki, J. Weaver-Feldhaus, M. McClure, J. F. Aitken, D. E. Anderson, W. Bergman, R. Frants, D. E. Goldgar, A. Green, R. MacLennan, N. G. Martin, L. J. Meyer, P. Youl, J. J. Zone, M. H. Skolnick
& L. A. Cannon-Albright doi:10.1038/ng0994-22 Abstract + references|PDF
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Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinomapp27 - 32 Carlos Caldas, Stephan A. Hahn, Luis T. da Costa, Mark S. Redston, Mieke Schutte, Albert B. Seymour, Craig L. Weinstein, Ralph H. Hruban, Charles J. Yeo
& Scott E. Kern doi:10.1038/ng0994-27 Abstract + references|PDF
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Human artificial episomal chromosomes for cloning large DNA fragments in human cellspp33 - 41 Tian-Qiang Sun, David A. Fenstermacher
& Jean-Michel H. Vos doi:10.1038/ng0994-33 Abstract + references|PDF
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Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosispp42 - 51 Ronald G. Crystal, Noel G. McElvaney, Melissa A. Rosenfeld, Chin-Shyan Chu, Andrea Mastrangeli, John G. Hay, Steven L. Brody, H. Ari Jaffe, N. Tony Eissa
& Claire Danel doi:10.1038/ng0994-42 Abstract + references|PDF
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Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control regionpp52 - 58 James S. Sutcliffe, Mitsuyoshi Nakao, Susan Christian, Karen H. Örstavik, Niels Tommerup, David H. Ledbetter
& Arthur L. Beaudet doi:10.1038/ng0994-52 Abstract + references|PDF
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Neomorphic agouti mutations in obese yellow micepp59 - 65 David M. J. Duhl, Harry Vrieling, Kimberly A. Miller, George L. Wolff
& Gregory S. Barsh doi:10.1038/ng0994-59 Abstract + references|PDF
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p53-deficient mice are extremely susceptible to radiation-induced tumorigenesispp66 - 69 Christopher J. Kemp, Tom Wheldon
& Allan Balmain doi:10.1038/ng0994-66 Abstract + references|PDF
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A radiation hybrid map of 506 STS markers spanning human chromosome 11pp70 - 76 M.R. James, C.W. Richard III, J.-J. Schott, C. Yousry, K. Clark, J. Bell, J.D. Terwilliger, J. Kazan, C. Dubay, A. Vignal, M. Agrapart, T. Imai, Y. Nakamura, M. Polymeropoulos, J. Weissenbach, D.R. Cox
& G.M. Lathrop doi:10.1038/ng0994-70 Abstract + references|PDF
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Identification of mutations in the 3(IV) and 4(IV) collagen genes in autosomal recessive Alport syndromepp77 - 82 Toshio Mochizuki, Henny H. Lemmink, Mariko Mariyama, Corinne Antignac, Marie-Claire Gubler, Yves Pirson, Christine Verellen-Dumoulin, Belinda Chan, Cornelis H. Schröder, Hubert J. Smeets
& Stephen T. Reeders doi:10.1038/ng0994-77 Abstract + references|PDF
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An autosomal locus causing autoimmune disease: autoimmune polyglandular disease type I assigned to chromosome 21pp83 - 87 Johanna Aaltonen, Petra Björses, Lodewijk Sandkuijl, Jaakko Perheentupa
& Leena Peltonen doi:10.1038/ng0994-83 Abstract + references|PDF
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Length of uninterrupted CGG repeats determines instability in the FMR1 genepp88 - 94 Evan E. Eichler, Jeanette J.A. Holden, Bradley W. Popovich, Allan L. Reiss, Karen Snow, Stephen N. Thibodeau, C. Sue Richards, Patricia A. Ward
& David L. Nelson doi:10.1038/ng0994-88 Abstract + references|PDF
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Linkage of the gene for Wolfram syndrome to markers on the short arm of chromosome 4pp95 - 97 Mihael H. Polymeropoulos, Ronnie Gorman Swift
& Michael Swift doi:10.1038/ng0994-95 Abstract + references|PDF
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Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndromepp98 - 103 William Reardon, Robin M. Winter, Paul Rutland, Louise J. Pulleyn, Barry M. Jones
& Sue Malcolm doi:10.1038/ng0994-98 Abstract + references|PDF
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The new common Markitsp104 Adrian J. Ivinson doi:10.1038/ng0994-104 Abstract|PDF
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3(IV) and 
