The early-onset torsion dystonia gene ( DYT1 ) encodes an ATP-binding protein von Ozelius, Laurie J, Hewett, Jeffrey W, Page, Curtis E, Bressman, Susan B, Kramer, Patricia L, Shalish, Christo, de Leon, Deborah, Brin, Mitchell F, Raymond, Deborah, Corey, David P, Fahn, Stanley, Risch, Neil J, Buckler, Alan J, Gusella, James F, Breakefield, Xandra O

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Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy von Harley, Helen G, Brook, J. David, Rundle, Shelley A, Crow, Stephen, Reardon, William, Buckler, Alan J, Harper, Peter S, Housman, David E, Shaw, Duncan J

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Isolation of genes from complex sources of mammalian genomic DNA using exon amplification von Church, Deanna M, Stotler, Christy J, Rutter, Joni L, Murrell, Jill R, Trofatter, James A, Buckler, Alan J

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Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury ( T ) gene family von Young, Ian D, Robson, Stephen C, Bonnet, Damien, Bullen, Philip J, Newbury-Ecob, Ruth A, Gebuhr, Tom, Buckler, Alan J, Wilson, David I, Law, David J, Terrett, Jonathan A, Brook, J. David, Yi Li, Quan, Strachan, Tom, Curtis, Andrew R.J, Raeburn, J. Alexander, Lyonnet, Stanislas, Ho Yi, Cheong

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Inactivating Mutations in an SH2 Domain-Encoding Gene in X-Linked Lymphoproliferative Syndrome von Nichols, Kim E., Harkin, D. Paul, Levitz, Seth, Krainer, Michael, Kolquist, Kathryn Ann, Genovese, Cameo, Bernard, Amy, Ferguson, Martin, Zuo, Lin, Snyder, Eric, Buckler, Alan J., Wise, Carol, Ashley, Jennifer, Lovett, Michael, Valentine, Marcus B., Look, A. Thomas, Gerald, William, Housman, David E., Haber, Daniel A.

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Isolation of a novel gene underlying batten disease, CLN3 von Lerner, Terry J, Boustany, Rose-Mary N, Anderson, John W, D'Arigo, Kenneth L, Schlumpf, Karen, Buckler, Alan J, Gusella, James F, Haines, Jonathan L

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Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member von Brook, J.David, McCurrach, Mila E., Harley, Helen G., Buckler, Alan J., Church, Deanna, Aburatani, Hiroyuki, Hunter, Kent, Stanton, Vincent P., Thirion, Jean-Paul, Hudson, Thomas, Sohn, Robert, Zemelman, Boris, Snell, Russell G., Rundle, Shelley A., Crow, Steve, Davies, June, Shelbourne, Peggy, Buxton, Jessica, Jones, Clare, Juvonen, Vesa, Johnson, Keith, Harper, Peter S., Shaw, Duncan J., Housman, David E.

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Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus von Call, Katherine M., Glaser, Tom, Ito, Caryn Y., Buckler, Alan J., Pelletier, Jerry, Haber, Daniel A., Rose, Elise A., Kral, Astrid, Yeger, Herman, Lewis, William H., Jones, Carol, Housman, David E.

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Exon Amplification: A Strategy to Isolate Mammalian Genes Based on RNA Splicing von BUCKLER, A. J, CHANG, D. D, GRAW, S. L, BROOK, J. D, HABER, D. A, SHARP, P. A, HOUSMAN, D. E

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Identification and characterization of novel human transcripts embedded within HMGA2 in t(12; 14)(q15; q24.1) uterine leiomyoma von Ingraham, SE, Lynch, R A, Surti, U, Rutter, J L, Buckler, A J, Khan, SA, Menon, A G, Lepont, P

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An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor von Haber, Daniel A., Buckler, Alan J., Glaser, Tom, Call, Katherine M., Pelletier, Jerry, Sohn, Robert L., Douglass, Edwin C., Housman, David E.

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Alternative Splicing and Genomic Structure of the Wilms Tumor Gene WT1 von Haber, Daniel A., Sohn, Robert L., Buckler, Alan J., Pelletier, Jerry, Call, Katherine M., Housman, David E.

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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes von MacDonald, Marcy E., Ambrose, Christine M., Duyao, Mabel P., Myers, Richard H., Lin, Carol, Srinidhi, Lakshmi, Barnes, Glenn, Taylor, Sherryl A., James, Marianne, Groot, Nicolet, MacFarlane, Heather, Jenkins, Barbara, Anderson, Mary Anne, Wexler, Nancy S., Gusella, James F., Bates, Gillian P., Baxendale, Sarah, Hummerich, Holger, Kirby, Susan, North, Mike, Youngman, Sandra, Mott, Richard, Zehetner, Gunther, Sedlacek, Zdenek, Poustka, Annemarie, Frischauf, Anna-Maria, Lehrach, Hans, Buckler, Alan J., Church, Deanna, Doucette-Stamm, Lynn, O'Donovan, Michael C., Riba-Ramirez, Laura, Shah, Manish, Stanton, Vincent P., Strobel, Scott A., Draths, Karen M., Wales, Jennifer L., Dervan, Peter, Housman, David E., Altherr, Michael, Shiang, Rita, Thompson, Leslie, Fielder, Thomas, Wasmuth, John J., Tagle, Danilo, Valdes, John, Elmer, Lawrence, Allard, Marc, Castilla, Lucio, Swaroop, Manju, Blanchard, Kris, Collins, Francis S., Snell, Russell, Holloway, Tracey, Gillespie, Kathleen, Datson, Nicole, Shaw, Duncan, Harper, Peter S.

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p16 Alterations and deletion mapping of 9p21-p22 in malignant mesothelioma von CHENG, J. Q, JHANWAR, S. C, KLEIN, W. M, BELL, D. W, LEE, W.-C, ALTOMARE, D. A, NOBORI, T, OLOPADE, O. I, BUCKLER, A. J, TESTA, J. R

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Expression of the Wilms' tumor gene WT1 in the murine urogenital system von PELLETIER, J, SCHALLING, M, BUCKLER, A. J, ROGERS, A, HABER, D. A, HOUSMAN, D

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p619, a giant protein related to the chromosome condensation regulator RCC1, stimulates guanine nucleotide exchange on ARF1 and Rab proteins von Rosa, J. L., Casaroli‐Marano, R. P., Buckler, A. J., Vilaró, S., Barbacid, M.

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Role of Rel-related factors in control of c-myc gene transcription in receptor-mediated apoptosis of the murine B cell WEHI 231 line von Lee, H, Arsura, M, Wu, M, Duyao, M, Buckler, A J, Sonenshein, G E

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Isolation, characterization, and expression of the murine Wilms' tumor gene (WT1) during kidney development von BUCKLER, A. J, PELLETIER, J, HABER, D. A, GLASER, T, HAUSMAN, D. E

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Interaction of an NF-κB-Like Factor with a Site Upstream of the C-MYC Promoter von Duyao, Mabel P., Buckler, Alan J., Sonenshein, Gail E.

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MTS1/CDKN2 gene mutations are rare in primary human astrocytomas with allelic loss of chromosome 9p von Ueki, Keisuke, Rubio, Mari-Paz, Ramesh, Vijaya, Correa, Katia M., Rutter, Joni L., Deimling, Andreas von, Buckler, Alan J., Gusella, James F., Louis, David N.

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