The structural and functional diversity of dystrophinpp283 - 291 Andrew H. Ahn
& Louis M. Kunkel doi:10.1038/ng0493-283 Abstract + references|PDF
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Chromosomal localization of seven PAX genes and cloning of a novel family member, PAX-9pp292 - 298 Paula Stapleton, Andreas Weith, Pavel Urbánek, Zbynek Kozmik
& Meinrad Busslinger doi:10.1038/ng0493-292 Abstract + references|PDF
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A mutation in the Pax-6 gene in rat small eye is associated with impaired migration of midbrain crest cellspp299 - 304 T. Matsuo, N. Osumi-Yamashita, S. Noji, H. Ohuchi, E. Koyama, F. Myokai, N. Matsuo, S. Taniguchi, H. Doi, S. Iseki, Y. Ninomiya, M. Fujiwara, T. Watanabe
& K. Eto doi:10.1038/ng0493-299 Abstract + references|PDF
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Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita)pp305 - 310 Alfred L. George Jr., Michael A. Crackower, Judith A. Abdalla, Arthur J. Hudson
& George C. Ebers doi:10.1038/ng0493-305 Abstract + references|PDF
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The cystic fibrosis mutation (F508) does not influence the chloride channel activity of CFTRpp311 - 316 Canhui Li, Mohabir Ramjeesingh, Evangelica Reyes, Tim Jensen, Xiubao Chang, Johanna M. Rommens
& Christine E. Bear doi:10.1038/ng0493-311 Abstract + references|PDF
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Clustered base substitutions in CTP synthetase conferring drug resistance in Chinese hamster ovary cellspp317 - 322 Jeremy Whelan, Geraldine Phear, Masatake Yamauchi
& Mark Meuth doi:10.1038/ng0493-317 Abstract + references|PDF
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Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defectpp323 - 326 Andreas Winterpacht, Matthias Hilbert, Ulrike Schwarze, Stefan Mundlos, Jürgen Spranger
& Bernhard U. Zabel doi:10.1038/ng0493-323 Abstract + references|PDF
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A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplexpp327 - 332 A. Hovnanian, E. Pollack, L. Hilal, A. Rochat, C. Prost, Y. Barrandon
& M. Goossens doi:10.1038/ng0493-327 Abstract + references|PDF
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A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3pp333 - 337 Hugh Watkins, Calum MacRae, Ludwig Thierfelder, Yah-Huei Chou, Michael Frenneaux, William McKenna, J.G. Seidman
& Christine E. Seidman doi:10.1038/ng0493-333 Abstract + references|PDF
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Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysispp338 - 341 Tuija Sulisalo, Pertti Sistonen2, Johanna Hästbacka, Claes Wadelius, Outi Mäkitie, Albert de la Chapelle
& Ilkka Kaitila doi:10.1038/ng0493-338 Abstract + references|PDF
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A gene for familial juvenile nephronophthisis (recessive medullary cystic kidney disease) maps to chromosome 2ppp342 - 345 Corinne Antignac, Christine H. Arduy, Jacques S. Beckmann, France Benessy, Françoise Gros, Monia Medhioub, Friedhelm Hildebrandt, Jean-Louis Dufier, Claire Kleinknecht, Michel Broyer, Jean Weissenbach, Renée Habib
& Daniel Cohen doi:10.1038/ng0493-342 Abstract + references|PDF
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Linkage of 11-hydroxylase mutations with altered steroid biosynthesis and blood pressure in the Dahl ratpp346 - 353 George T. Cicila, John P. Rapp, Jia-Ming Wang, Elizabeth St. Lezin, Shi Chung Ng
& Theodore W. Kurtz doi:10.1038/ng0493-346 Abstract + references|PDF
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Genetic determinants of diastolic and pulse pressure map to different loci in Lyon hypertensive ratspp354 - 357 Christopher Dubay, Madeleine Vincent, Nilesh J. Samani, Pascale Hilbert, Michael A. Kaiser, Jean-Paul Beressi, Yuri Kotelevtsev, Jacques S. Beckmann, Florent Soubrier, Jean Sassard
& G. Mark Lathrop doi:10.1038/ng0493-354 Abstract + references|PDF
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HLA class II alleles and susceptibility and resistance to insulin dependent diabetes mellitus in Mexican-American familiespp358 - 364 Henry A. Erlich, Adina Zeidler, Julie Chang, Sylvia Shaw, Leslie J. Raffel, William Klitz, Yolanda Beshkov, Gertrude Costin, Sheila Pressman, Teodorica Bugawan
& Jerome I. Rotter doi:10.1038/ng0493-358 Abstract + references|PDF
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Targeting in linear DNA duplexes with two complementary probe strands for hybrid stabilitypp365 - 372 Elissa P. Sena
& David A. Zarling doi:10.1038/ng0493-365 Abstract + references|PDF
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F508) does not influence the chloride channel activity of CFTR
-hydroxylase mutations with altered steroid biosynthesis and blood pressure in the Dahl rat
