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Rescue of erythroid development in gene targeted GATA−1- mouse embryonic stem cellspp92 - 98 M. Celeste Simon, Larysa Pevny, Michael V. Wiles, Gordon Keller, Frank Costantini
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The Huntington's disease candidate region exhibits many different haplotypespp99 - 103 Marcy E. MacDonald, Andrea Novelletto, Carol Lin, Dan Tagle, Glenn Barnes, Gillian Bates, Sherry Taylor, Bernice Allitto, Michael Altherr, Richard Myers, Hans Lehrach, Francis S. Collins, John J. Wasmuth, Marina Frontali
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Exclusion of DNA changes in the −subunit of the c−GMP phosphodiesterase gene as the cause for Huntington's diseasepp104 - 108 Olaf Riess, Anne Noerremoelle, Colin Collins, Diana Mah, Bernhard Weber
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Aberrant splicing of the CHM gene is a significant cause of choroideremiapp109 - 113 Eeva-Marja Sankila, Ritva Tolvanen, José A. J. M. van den Hurk, Frans P. M. Cremers
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A survey of expressed genes in Caenorhabditis eleganspp114 - 123 R. Waterston, C. Martin, M. Craxton, C. Huynh, A. Coulson, L. Hillier, R. Durbin, P. Green, R. Shownkeen, N. Halloran, M. Metzstein, T. Hawkins, R. Wilson, M. Berks, Z. Du, K. Thomas, J. Thierry-Mieg
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Caenorhabditis elegans expressed sequence tags identify gene families and potential disease gene homologuespp124 - 131 W. Richard McCombie, Mark D. Adams, Jenny M. Kelley, Michael G. FitzGerald, Teresa R. Utterback, Mohammad Khan, Mark Dubnick, Anthony R. Kerlavage, J. Craig Venter
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Construction of a mouse yeast artificial chromosome library in a recombination−deficient strain of yeastpp132 - 136 F. L. Chartier, J. T. Keer, M. J. Sutcliffe, D. A. Henriques, P. Mileham
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A novel GC−rich human macrosatellite VNTR in Xq24 is differentially methylated on active and inactive X chromosomespp137 - 143 Joseph Giacalone, Jonathan Friedes
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Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital developmentpp144 - 148 Wendy Bruening, Nabeel Bardeesy, Bernard L. Silverman, Richard A. Cohn, Geoffrey A. Machin, Andrew J. Aronson, David Housman
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A donor splice site mutation in the parathyroid hormone gene is associated with autosomal recessive hypoparathyroidismpp149 - 152 David B. Parkinson
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subunit multigene family
−subunit of the c−GMP phosphodiesterase gene as the cause for Huntington's disease
