Rezultati - Sanger, Warren G.

INCREASED FREQUENCY OF SISTER-CHROMATID EXCHANGES IN ALCOHOLICS od BUTLER, MERLIN G., SANGER, WARREN G., VEOMETT, GEORGE E.

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A Possible Etiology Of The Infertile 46XX Male Subject od Butler, Merlin G., Walzak, Myron P., Sanger, Warren G., Todd, Curtis T.

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Additional Evidence for X-Y Chromosome Interchange in a 46,XX Male od BUTLER, MERLIN G., WALZAK, MYRON P., SANGER, WARREN G., TODD, CURTIS T.

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Autistic and Dysmorphic Features Associated With a Submicroscopic 2q33.3—q34 Interstitial Deletion Detected by Array Comparative Genomic Hybridization od Brandau, Duane T., Lund, Molly, Cooley, Linda D., Sanger, Warren G., Butler, Merlin G.

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Extranodal marginal zone lymphoma of the dura mater with IgH/MALT1 translocation and review of literature od Bhagavathi, Sharathkumar, Greiner, Timothy C., Kazmi, Syed A., Fu, Kai, Sanger, Warren G., Chan, Wing C.

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Characterization of Childhood Precursor T-Lymphoblastic Lymphoma by Immunophenotyping and Fluorescent In-Situ Hybridization: A Report from the Children’s Oncology Group od Smock, Kristi J., Nelson, Marilu, Tripp, Sheryl R., Sanger, Warren G., Abromowitch, Minnie, Cairo, Mitchell S., Perkins, Sherrie L.

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Gene targeting in adult rhesus macaque fibroblasts od Meehan, Daniel T, Zink, Mary Ann, Mahlen, Melissa, Nelson, Marilu, Sanger, Warren G, Mitalipov, Shoukhrat M, Wolf, Don P, Ouellette, Michel M, Norgren, Robert B

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Characterization of Clonality of Epstein-Barr Virus-Induced Human B Lymphoproliferative Disease in Mice with Severe Combined Immunodeficiency od Nakamine, Hirokazu, Masih, Aneal S., Okano, Motohiko, Taguchi, Yuichi, Pirruccello, Samuel J., Davis, Jack R., Mahloch, Mark L., Beisel, Kirk W., Kleveland, Kimberly, Sanger, Warren G., Purtilo, David T.

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Large Contiguous Gene Deletions in Sjögren-Larsson Syndrome od Engelstad, Holly, Carney, Gael, S'Aulis, Dana, Rise, Janae, Sanger, Warren G., Rudd, M. Katharine, Richard, Gabriele, Carr, Christopher W., Abdul-Rahman, Omar A., Rizzo, William B.

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Cytosine Arabinoside and Mitoxantrone Followed by Second Allogeneic Transplant for the Treatment of Children With Refractory Juvenile Myelomonocytic Leukemia od Patel, Sachit A., Coulter, Don W., Grovas, Alfred C., Gordon, Bruce G., Harper, James L., Warkentin, Phyllis I., Wisecarver, James L., Sanger, Warren G., Coccia, Peter F.

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t(14;18)-negative Follicular Lymphomas Are Associated with a High Frequency of BCL6 Rearrangement at the Alternative Breakpoint Region od Gu, Keni, Fu, Kai, Jain, Smrati, Liu, Zhongfen, Iqbal, Javeed, Li, Min, Sanger, Warren G, Weisenburger, Dennis D, Greiner, Timothy C, Aoun, Patricia, Dave, Bhavana J, Chan, Wing C

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An increased frequency of 13q deletions detected by fluorescence in situ hybridization and its impact on survival in children and adolescents with Burkitt lymphoma: results from th... od Nelson, Marilu, Perkins, Sherrie L., Dave, Bhavana J., Coccia, Peter F., Bridge, Julia A., Lyden, Elizabeth R., Heerema, Nyla A., Lones, Mark A., Harrison, Lauren, Cairo, Mitchell S., Sanger, Warren G.

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Genome Wide Copy Number Analysis of Paediatric Burkitt Lymphoma Using Formalin-Fixed Tissues Reveals a Subset with Gain of Chromosome 13q and Corresponding miRNA Over Expression od Schiffman, Joshua D., Lorimer, Patrick D., Rodic, Vladimir, Jahromi, Mona S., Downie, Jonathan M., Bayerl, Michael G., Sanmann, Jennifer N., Althof, Pamela A., Sanger, Warren G., Barnette, Phillip, Perkins, Sherrie L., Miles, Rodney R.

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Primary Follicular Lymphoma of the Testis in Children and Adolescents od Lones, Mark A., Raphael, Martine, McCarthy, Keith, Wotherspoon, Andrew, Terrier-Lacombe, Marie-Josee, Ramsay, Alan D., MacLennan, Ken, Cairo, Mitchell S., Gerrard, Mary, Michon, Jean, Patte, Catherine, Pinkerton, Ross, Sender, Leonard, Auperin, Anne, Sposto, Richard, Weston, Claire, Heerema, Nyla A., Sanger, Warren G., von Allmen, Daniel, Perkins, Sherrie L.

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Molecular Characteristics of Mantle Cell Lymphoma Presenting with Clonal Plasma Cell Component od Visco, Carlo, Hoeller, Sylvia, Malik, Jeffrey T., Xu-Monette, Zijun Y., Wiggins, Michele L., Liu, Jessica, Sanger, Warren G., Liu, Zhongfeng, Chang, Julie, Ranheim, Erik A., Gradowski, Joel F., Serrrano, Sergio, Wang, Huan-You, Liu, Qingquan, Dave, Sandeep, Olsen, Brian, Gascoyne, Randy D., Campo, Elias, Swerdlow, Steven H., Chan, Wing C., Tzankov, Alexander, Young, Ken H.

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Cyclin D1–negative mantle cell lymphoma: a clinicopathologic study based on gene expression profiling od Fu, Kai, Weisenburger, Dennis D., Greiner, Timothy C., Dave, Sandeep, Wright, George, Rosenwald, Andreas, Chiorazzi, Michael, Iqbal, Javeed, Gesk, Stefan, Siebert, Reiner, De Jong, Daphne, Jaffe, Elaine S., Wilson, Wyndham H., Delabie, Jan, Ott, German, Dave, Bhavana J., Sanger, Warren G., Smith, Lynette M., Rimsza, Lisa, Braziel, Rita M., Müller-Hermelink, H. Konrad, Campo, Elias, Gascoyne, Randy D., Staudt, Louis M., Chan, Wing C.

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BCL2 Translocation Defines a Unique Tumor Subset within the Germinal Center B-Cell-Like Diffuse Large B-Cell Lymphoma od Iqbal, Javeed, Sanger, Warren G., Horsman, Douglas E., Rosenwald, Andreas, Pickering, Diane L., Dave, Bhavana, Dave, Sandeep, Xiao, Li, Cao, Kajia, Zhu, Quiming, Sherman, Simon, Hans, Christine P., Weisenburger, Dennis D., Greiner, Timothy C., Gascoyne, Randy D., Ott, German, Müller-Hermelink, H. Konrad, Delabie, Jan, Braziel, Rita M., Jaffe, Elaine S., Campo, Elias, Lynch, James C., Connors, Joseph M., Vose, Julie M., Armitage, James O., Grogan, Thomas M., Staudt, Louis M., Chan, Wing C.

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Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia od Moreno-De-Luca, Daniel, Mulle, Jennifer G., Kaminsky, Erin B., Sanders, Stephan J., Myers, Scott M., Adam, Margaret P., Pakula, Amy T., Eisenhauer, Nancy J., Uhas, Kim, Weik, LuAnn, Guy, Lisa, Care, Melanie E., Morel, Chantal F., Boni, Charlotte, Salbert, Bonnie Anne, Chandrareddy, Ashadeep, Demmer, Laurie A., Chow, Eva W.C., Surti, Urvashi, Aradhya, Swaroop, Pickering, Diane L., Golden, Denae M., Sanger, Warren G., Aston, Emily, Brothman, Arthur R., Gliem, Troy J., Thorland, Erik C., Ackley, Todd, Iyer, Ram, Huang, Shuwen, Barber, John C., Crolla, John A., Warren, Stephen T., Martin, Christa L., Ledbetter, David H.

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Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia od Moreno-De-Luca, Daniel, Mulle, Jennifer G., Kaminsky, Erin B., Sanders, Stephan J., Myers, Scott M., Adam, Margaret P., Pakula, Amy T., Eisenhauer, Nancy J., Uhas, Kim, Weik, LuAnn, Guy, Lisa, Care, Melanie E., Morel, Chantal F., Boni, Charlotte, Salbert, Bonnie Anne, Chandrareddy, Ashadeep, Demmer, Laurie A., Chow, Eva W.C., Surti, Urvashi, Aradhya, Swaroop, Pickering, Diane L., Golden, Denae M., Sanger, Warren G., Aston, Emily, Brothman, Arthur R., Gliem, Troy J., Thorland, Erik C., Ackley, Todd, Iyer, Ram, Huang, Shuwen, Barber, John C., Crolla, John A., Warren, Stephen T., Martin, Christa L., Ledbetter, David H.

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An evidence-based approach to establish the functional and clinical significance of CNVs in intellectual and developmental disabilities od Kaminsky, Erin B., Kaul, Vineith, Paschall, Justin, Church, Deanna M., Bunke, Brian, Kunig, Dawn, Moreno-De-Luca, Daniel, Moreno-De-Luca, Andres, Mulle, Jennifer G., Warren, Stephen T., Richard, Gabriele, Compton, John G., Fuller, Amy E., Gliem, Troy J., Huang, Shuwen, Collinson, Morag N., Beal, Sarah J., Ackley, Todd, Pickering, Diane L., Golden, Denae M., Aston, Emily, Whitby, Heidi, Shetty, Shashirekha, Rossi, Michael R., Rudd, M. Katharine, South, Sarah T., Brothman, Arthur R., Sanger, Warren G., Iyer, Ramaswamy K., Crolla, John A., Thorland, Erik C., Aradhya, Swaroop, Ledbetter, David H., Martin, Christa L.

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