Meiotic drive at the myotonic dystrophy locus?pp117 - 118 Nessa Carey, Keith Johnson, Pekka Nokelainen, Leena Peltonen, Maria-Liisa Savontaus, Vesa Juvonen, Maria Anvret, Ulla Grandell, Kokila Chotai, Elaine Robertson, Helen Middleton-Price
& Sue Malcolm doi:10.1038/ng0294-117 References|PDF
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Issues in searching molecular sequence databasespp119 - 129 Stephen F. Altschul, Mark S. Boguski, Warren Gish
& John C. Wootton doi:10.1038/ng0294-119 Abstract + references|PDF
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Identification of the remains of the Romanov family by DNA analysispp130 - 135 Peter Gill, Pavel L. Ivanov, Colin Kimpton, Romelle Piercy, Nicola Benson, Gillian Tully, Ian Evett, Erika Hagelberg
& Kevin Sullivan doi:10.1038/ng0294-130 Abstract + references|PDF
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Complex gene conversion events in germline mutation at human minisatellitespp136 - 145 Alec J. Jeffreys, Keiji Tamaki, Annette MacLeod, Darren G. Monckton, David L. Neil
& John A.L. Armour doi:10.1038/ng0294-136 Abstract + references|PDF
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A second Ewing's sarcoma translocation, t(21;22), fuses the EWS gene to another ETS−family transcription factor, ERGpp146 - 151 Poul H.B. Sorensen, Stephen L. Lessnick, Dolores Lopez-Terrada, Xian F. Liu, Timothy J. Triche
& Christopher T. Denny doi:10.1038/ng0294-146 Abstract + references|PDF
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Instability of short tandem repeats (microsatellites) in human cancerspp152 - 156 R. Wooster, A.-M. Cleton-Jansen, N. Collins, J. Mangion, R.S. Cornelis, C.S. Cooper, B.A. Gusterson, B.A.J. Ponder, A. von Deimling, O.D. Wiestler, C.J. Cornelisse, P. Devilee
& M.R. Stratton doi:10.1038/ng0294-152 Abstract + references|PDF
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HLA DR−DQ associations with cervical carcinoma show papillomavirus−type specificitypp157 - 162 Raymond J. Apple, Henry A. Erlich, William Klitz, M. Michele Manos, Thomas M. Becker
& Cosette M. Wheeler doi:10.1038/ng0294-157 Abstract + references|PDF
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Maternal imprinting of human SNRPN, a gene deleted in Prader−Willi syndromepp163 - 167 Martha L. Reed
& Stuart E. Leff doi:10.1038/ng0294-163 Abstract + references|PDF
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Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomalypp168 - 173 Isabel M. Hanson, Judy M. Fletcher, Tim Jordan, Alison Brown, David Taylor, Rebecca J. Adams, Hope H. Punnett
& Veronica van Heyningen doi:10.1038/ng0294-168 Abstract + references|PDF
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Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK)pp174 - 179 André Reis, Hans-Christian Hennies, Lutz Langbein, Martin Digweed, Dietmar Mischke, Matthias Drechsler, Evelin Schröck, Brigitte Royer-Pokora, Werner W. Franke, Karl Sperling
& Wolfang Küster doi:10.1038/ng0294-174 Abstract + references|PDF
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Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomaspp180 - 184 Martin H. Ruttledge, Julie Sarrazin, Shyam Rangaratnam, Catherine M. Phelan, Elspeth Twist, Philippe Merel, Olivier Delattre, Gilles Thomas, Magnus Nordenskjöld, V. Peter Collins, Jan P. Dumanski
& Guy A. Rouleau doi:10.1038/ng0294-180 Abstract + references|PDF
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Mutations in transcript isoforms of the neurofibromatosis 2 gene in multiple human tumour typespp185 - 192 Albert B. Bianchi, Tetsuo Hara, Vijaya Ramesh, Jizong Gao, Andrés J. P. Klein-Szanto, Francine Morin, Anil G. Menon, James A. Trofatter, James F. Gusella, Bernd R. Seizinger
& Nikolai Kley doi:10.1038/ng0294-185 Abstract + references|PDF
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Loss of heterozygosity on chromosome 16p13.3 in hamartomas from tuberous sclerosis patientspp193 - 196 Andrew J. Green, Moyra Smith
& John R.W. Yates doi:10.1038/ng0294-193 Abstract + references|PDF
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A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33−34pp197 - 204 M.T. McDonald, K.A. Papenberg, S. Ghosh, A.A. Glatfelter, B.B. Biesecker, E.A. Helmbold, D.S. Markel, A. Zolotor, W.C. McKinnon, J.L. Vanderstoep, C.E. Jackson, M. Iannuzzi, F.S. Collins, M. Boehnke, M.E. Porteous, A.E. Guttmacher
& D.A. Marchuk doi:10.1038/ng0294-197 Abstract + references|PDF
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A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3pp205 - 209 Claire L. Shovlin, J.M.B. Hughes, E.G.D. Tuddenham, I. Temperley, Y.F.N. Perembelon, J. Scott, Christine E. Seidman
& J.G. Seidman doi:10.1038/ng0294-205 Abstract + references|PDF
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Genetic linkage of cone−rod retinal dystrophy to chromosome 19q and evidence for segregation distortionpp210 - 213 Kevin Evans, Alan Fryer, Christopher Inglehearn, Josephine Duvall-Young, Joanne L. Whittaker, Cheryl Y. Gregory, Rachel Butler, Neil Ebenezer, David M. Hunt
& Shomi Bhattacharya doi:10.1038/ng0294-210 Abstract + references|PDF
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Corrigendum: The Wilson disease gene is a putative copper transporting P−type ATPase similar to the Menkes genep214 doi:10.1038/ng0294-214a PDF
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Corrigendum: A gene for Stargardt's disease (fundus flavimaculatus) maps to the short arm of chromosome 1p214 doi:10.1038/ng0294-214b PDF
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Corrigendum: Reduced transcriptional regulatory competence of the androgen receptor in X−linked spinal and bulbar muscular atrophyp214 doi:10.1038/ng0294-214c PDF
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Corrigendum: Fusion of a fork head domain gene to PAX3 in the solid tumour alveolar rhabdomyosarcomap214 doi:10.1038/ng0294-214d PDF
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