Mutations of PAX3 unlikely in Waardenburg syndrome type 2p8 Sergio Arias doi:10.1038/ng0993-8a References|PDF
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Reply to "Mutations of PAX3 unlikely in Waardenburg syndrome type 2"p8 Andrew P. Read, Valerie Newton
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Anticipation in spinocerebellar ataxia type 2pp8 - 10 Stefan-M. Pulst, Alex Nechiporuk
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Hemizygosity at the elastin locus in a developmental disorder, Williams syndromepp11 - 16 Amanda K. Ewart, Colleen A. Morris, Donald Atkinson, Weishan Jin, Keith Sternes, Patricia Spallone, A. Dean Stock, Mark Leppert
& Mark T. Keating doi:10.1038/ng0993-11 Abstract + references|PDF
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High resolution visual mapping of stretched DNA by fluorescent hybridizationpp17 - 21 Irma Parra
& Bradford Windle doi:10.1038/ng0993-17 Abstract + references|PDF
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Introduction and expression of the 400 kilobase precursor amyloid protein gene in transgenic micepp22 - 30 Bruce T. Lamb, Sangram S. Sisodia, Ann M. Lawler, Hilda H. Slunt, Cheryl A. Kitt, William G. Kearns, Peter L. Pearson, Donald L. Price
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Charcot−Marie−Tooth neuropathy type 1B is associated with mutations of the myelin P0 genepp31 - 34 Kiyoshi Hayasaka, Masato Himoro, Wataru Sato, Goro Takada, Keiichi Uyemura, Nobuyoshi Shimizu, Thomas D. Bird, P. Michael Conneally
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Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot−Marie−Tooth disease type 1Bpp35 - 39 Tanja Kulkens, Pieter A. Bolhuis, Ruud A. Wolterman, Stephan Kemp, Saskia te Nijenhuis, Linda J. Valentijn, Gerard W. Hensels, Frans G.I. Jennekens, Marianne de Visser, Jessica E. Hoogendijk
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A gene for familial hemiplegic migraine maps to chromosome 19pp40 - 45 Anne Joutel, Marie-Germaine Bousser, Valérie Biousse, Pierre Labauge, Hugues Chabriat, Argentino Nibbio, Jacqueline Maciazek, Bénédicte Meyer, Marie-Anne Bach, Jean Weissenbach, G. Mark Lathrop
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A mutation in the human ryanodine receptor gene associated with central core diseasepp46 - 50 Yilin Zhang, Hai Shiene Chen, Vijay K. Khanna, Stella De Leon, Michael S. Phillips, Keith Schappert, Beverley A. Britt, A. Keith W. Brownell
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Mutations in the ryanodine receptor gene in central core disease and malignant hyperthermiapp51 - 55 K. A. Quane, J.M.S. Healy, K. E. Keating, B. M. Manning, F. J. Couch, L. M. Palmucci, C. Doriguzzi, T. H. Fagerlund, K. Berg, H. Ording, D. Bendixen, W. Mortier, U. Linz, C. R. Muller
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Point mutations in the c−Myc transactivation domain are common in Burkitt's lymphoma and mouse plasmacytomaspp56 - 61 K. Bhatia, K. Huppi, G. Spangler, D. Siwarski, R. Iyer
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Molecular genetic basis of the human Rhesus blood group systempp62 - 65 Isabelle Mouro, Yves Colin, Baya Chérif-Zahar, Jean-Pierre Cartron
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LAZ3, a novel zinc−finger encoding gene, is disrupted by recurring chromosome 3q27 translocations in human lymphomaspp66 - 70 Jean-Pierre Kerckaert, Clotilde Deweindt, Hervé Tilly, Sabine Quief, Gérard Lecocq
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Homozygous deletion of the human insulin receptor gene results in leprechaunismpp71 - 73 Efrat Wertheimer, Su-Ping Lu, Philippe F. Backeljauw, Marsha L. Davenport
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The insulin−like growth factor type−2 receptor gene is imprinted in the mouse but not in humanspp74 - 78 Vera M. Kalscheuer, Edwin C. Mariman, Marga T. Schepens, Helga Rehder
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A type X collagen mutation causes Schmid metaphyseal chondrodysplasiapp79 - 82 Matthew L. Warman, Margaret Abbott, Suneel S. Apte, Tim Hefferon, Iain McIntosh, Daniel H. Cohn, Jacqueline T. Hecht, Bjorn R. Olsen
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Primary amenorrhoea and infertility due to a mutation in the −subunit of follicle−stimulating hormonepp83 - 86 C.H. Matthews, S. Borgato, P. Beck-Peccoz, M. Adams, Y. Tone, G. Gambino, S. Casagrande, G. Tedeschini, A. Benedetti
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Mapping loci influencing the persistence of Theiler's virus in the murine central nervous systempp87 - 91 Jean-François Bureau, Xavier Montagutelli, Franck Bihl, Suzie Lefebvre, Jean-Louis Guénet
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Mouse minisatellite mutations induced by ionizing radiationpp92 - 94 Yuri E. Dubrova, Alec J. Jeffreys
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Isolation and characterization of APLP2 encoding a homologue of the Alzheimer's associated amyloid protein precursorpp95 - 100 Wilma Wasco, Sarada Gurubhagavatula, Marc d. Paradis, Donna M. Romano, Sangram S. Sisodia, Bradley T. Hyman, Rachael L. Neve
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−subunit of follicle−stimulating hormone
