Výsledky vyhledávání - Sanger, Warren G.

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

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A Possible Etiology Of The Infertile 46XX Male Subject Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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... Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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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