How neutral are synonymous codon mutations?p259 Isabella Richard
& Jacques S. Beckmann doi:10.1038/ng0795-259 References|PDF
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Atopy in Australiap260 David L. Duffy, Sue C. Healey, Georgia Chenevix-Trench, Nick G. Martin, John Weger
& Jay Lichter doi:10.1038/ng0795-260a References|PDF
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Reply to "Atopy in Australia"p260 Michael R. Hill
& William O. Cookson doi:10.1038/ng0795-260b References|PDF
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Analysis of the nucleotide sequence of chromosome VI from Saccharomyces cerevisiaepp261 - 268 Yasufumi Murakami, Masanori Naitou, Hiroko Hagiwara, Takehiko Shibata, Masashi Ozawa, Syun-ichi Sasanuma, Motoe Sasanuma, Yukari Tsuchiya, Eiichi Soeda, Kazushige Yokoyama, Masaaki Yamazaki, Hiroyuki Tashiro
& Toshihiko Eki doi:10.1038/ng0795-261 Abstract + references|PDF
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Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate genepp269 - 278 Marcia L. Budarf, Joelle Collins, Weilong Gong, Bruce Roe, Zhili Wang, L. Charles Bailey, Bea Sellinger, Dominique Michaud, Deborah A. Driscoll
& Beverly S. Emanuel doi:10.1038/ng0795-269 Abstract + references|PDF
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Adenosine−deaminase−deficient mice die perinatally and exhibit liver−cell degeneration, atelectasis and small intestinal cell deathpp279 - 287 Alexandra A.J. Migchielsen, Marco L. Breuer, Marian A. van Roon, Hein te Riele, Chris Zurcher, Ferry Ossendorp, Stephan Toutain, Michael S. Hershfield, Anton Berns
& Dinko Valerio doi:10.1038/ng0795-279 Abstract + references|PDF
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Acid sphingomyelinase deficient mice: a model of types A and B Niemann−Pick diseasepp288 - 293 Kenichi Horinouchi, Shai Erlich, Daniel P. Perl, Klaus Ferlinz, Charles L. Bisgaier, Konrad Sandhoff, Robert J. Desnick, Colin L. Stewart
& Edward H. Schuchman doi:10.1038/ng0795-288 Abstract + references|PDF
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The Grb2 binding domain of mSos1 is not required for downstream signal transductionpp294 - 300 Wei Wang, Elizabeth M.C. Fisher, Qi Jia, James M. Dunn, Emilio Porfiri, Julian Downward
& Sean E. Egan doi:10.1038/ng0795-294 Abstract + references|PDF
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The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1pp301 - 306 Arthur Brown, Gilbert Bernier, Martine Mathieu, Janet Rossant
& Rashmi Kothary doi:10.1038/ng0795-301 Abstract + references|PDF
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Cloning of the galactokinase cDNA and identification of mutations in two families with cataractspp307 - 312 Dwight Stambolian, Yunjun Ai, Duska Sidjanin, Kristin Nesburn, Ganesh Sathe, Martin Rosenberg
& Derk J. Bergsma doi:10.1038/ng0795-307 Abstract + references|PDF
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Identification of murine loci associated with susceptibility to chronic experimental autoimmune encephalomyelitispp313 - 317 Mats Sundvall, Johan Jirholt, Hai-Tao Yang, Liselotte Jansson, Åke Engström, Ulf Pettersson
& Rikard Holmdahl doi:10.1038/ng0795-313 Abstract + references|PDF
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Establishment of functional imprinting of the H19 gene in human developing placentaepp318 - 324 Yoshihiro Jinno, Yuichiro Ikeda, Kankatsu Yun, Marion Maw, Hideaki Masuzaki, Hisanobu Fukuda, Kunihiko Inuzuka, Akira Fujishita, Yoshinobu Ohtani, Tomoaki Okimoto, Tadayuki Ishimaru
& Norio Niikawa doi:10.1038/ng0795-318 Abstract + references|PDF
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Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasiapp325 - 329 Jacqueline T. Hecht, Laura D. Nelson, Eric Crowder, Yang Wang, Frederick F.B. Elder, Wilbur R. Harrison, Clair A. Francomano, Christa K. Prange, Gregory G. Lennon, Michelle Deere
& Jack Lawler doi:10.1038/ng0795-325 Abstract + references|PDF
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Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein genepp330 - 336 M.D. Briggs, S.M.G. Hoffman, L.M. King, A.S. Olsen, H. Mohrenweiser, J.G. Leroy, G.R. Mortier, D.L. Rimoin, R.S. Lachman, E.S. Gaines, J.A. Cekleniak, R.G. Knowlton
& D.H. Cohn doi:10.1038/ng0795-330 Abstract + references|PDF
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Microsatellite evolution — evidence for directionality and variation in rate between speciespp337 - 343 David C. Rubinsztein, William Amos, Jayne Leggo, Sandy Goodburn, Sanjeev Jain, Shi-Hua Li, Russell L. Margolis, Christopher A. Ross
& Malcolm A. Ferguson-Smith doi:10.1038/ng0795-337 Abstract + references|PDF
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Gametic and somatic tissue−specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1pp344 - 350 Samuel S. Chong, Alanna E. McCall, Juan Cota, S.H. Subramony, Harry T. Orr, Mark R. Hughes
& Huda Y. Zoghbi doi:10.1038/ng0795-344 Abstract + references|PDF
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Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindredspp351 - 353 Nelleke A. Gruis, Pieter A. van der Velden, Lodewijk A. Sandkuijl, Duncan E. Prins, Jane Weaver-Feldhaus, Alexander Kamb, Wilma Bergman
& Rune R. Frants doi:10.1038/ng0795-351 Abstract + references|PDF
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Assignment of dominant inherited nocturnal enuresis (ENUR1) to chromosome 13qpp354 - 356 Hans Eiberg, Ida Berendt
& Jan Mohr doi:10.1038/ng0795-354 Abstract + references|PDF
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A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasiapp357 - 359 Gary A. Bellus, Iain McIntosh, E. Anne Smith, Arthur S. Aylsworth, Ilkka Kaitila, William A. Horton, Giselle A. Greenhaw, Jacqueline T. Hecht
& Clair A. Francomano doi:10.1038/ng0795-357 Abstract + references|PDF
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A homozygous 1−base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanesepp360 - 362 Sigrid Fuchs, Mitsuru Nakazawa, Marion Maw, Makoto Tamai, Yoshihisa Oguchi
& Andreas Gal doi:10.1038/ng0795-360 Abstract + references|PDF
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Mutation of a type II keratin gene (K6a) in pachyonychia congenitapp363 - 365 Paul E. Bowden, Joanne L. Haley, Aleksej Kansky, Joseph A. Rothnagel, David O. Jones
& Richard J. Turner doi:10.1038/ng0795-363 Abstract + references|PDF
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