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Blood, ISSN 0006-4971, 11/2018, Volume 132, Issue Supplement 1, pp. 5576 - 5576
Abstract Background Monoclonal gammopathy of undetermined significance (MGUS) is an asymptomatic condition arising from clonal plasma cells and has the risk of... 
Journal Article
Cytometry Part B: Clinical Cytometry, ISSN 1552-4949, 01/2016, Volume 90, Issue 1, pp. 11 - 13
Journal Article
Cytometry Part B: Clinical Cytometry, ISSN 1552-4949, 01/2016, Volume 90, Issue 1, pp. 2 - 2
Journal Article
Blood, ISSN 0006-4971, 12/2011, Volume 118, Issue 25, pp. 6480 - 6481
In this issue of Blood, Fazi and colleagues have asked important questions and added several new observations to our understanding of monoclonal B-cell... 
NUMBERS | HEMATOLOGY | B-CELL LYMPHOCYTOSIS
Journal Article
Cytometry Part B: Clinical Cytometry, ISSN 1552-4949, 09/2013, Volume 84, Issue 5, pp. 339 - 341
Journal Article
Cytometry Part B: Clinical Cytometry, ISSN 1552-4949, 09/2013, Volume 84, Issue 5, pp. 350 - 353
Journal Article
Cytometry Part B: Clinical Cytometry, ISSN 1552-4949, 09/2013, Volume 84, Issue 5, pp. 346 - 349
Journal Article
Blood, ISSN 0006-4971, 11/2015, Volume 126, Issue 19, pp. 2213 - 2219
Journal Article
Blood, ISSN 0006-4971, 05/2018, Volume 131, Issue 21, pp. 2357 - 2366
The safety and efficacy of ibrutinib (420 mg) in chronic lymphocytic leukemia (CLL) were evaluated in a phase 2 study; 51 patients had aberration (TP53 cohort)... 
Lymphoid Neoplasia
Journal Article
Blood, ISSN 0006-4971, 11/2011, Volume 118, Issue 21, pp. 3881 - 3881
Abstract Abstract 3881 Background: Chronic lymphocytic leukemia (CLL) is largely incurable neoplasm of the blood and has one of the highest familial risks of... 
Journal Article
Blood, ISSN 0006-4971, 11/2009, Volume 114, Issue 22, pp. 4391 - 4391
Abstract Abstract 4391 Introduction The Recently described NZB miRNA15a/16-1 mutation is syntenic to 13q14 deletion in CLL. The mir15a/16-1 complex is thought... 
Journal Article
Cancer Research, ISSN 0008-5472, 04/2010, Volume 70, Issue 8 Supplement, pp. 323 - 323
Journal Article
by Brooks-Wilson, Angela and Liu, Jianjun and Nieters, Alexandra and Camp, Nicola J and Rabe, Kari G and Lan, Qing and de Sanjosé, Silvia and Smith, Martyn T and Adami, Hans-Olov and Humphreys, Keith and Spinelli, John J and Halperin, Eran and Call, Timothy G and Boffetta, Paolo and Butterbach, Katja and Conde, Lucia and Akers, Nicholas K and Holly, Elizabeth A and Agana, Luz and Hjalgrim, Henrik and Glenn, Martha and Boyle, Peter and Zheng, Tongzhang and Rassenti, Laura Z and Smedby, Karin E and Cocco, Pierluigi and Milliken, Sam and Lanasa, Mark C and Cerhan, James R and Zahm, Shelia H and Slager, Susan L and Cunningham, Julie M and Darabi, Hatef and Davis, Scott and Cozen, Wendy and Purdue, Mark P and Foretova, Lenka and Maynadié, Marc and Strom, Sara S and Goldin, Lynn R and Zhang, Yawei and Kay, Neil E and Melbye, Mads and Staines, Anthony and Hartge, Patricia and Benavente, Yolanda and Kricker, Anne and Caporaso, Neil E and Becker, Nikolaus and Wang, Sophia S and Bracci, Paige M and Glimelius, Bengt and Marti, Gerald E and Chang, Ellen T and Riby, Jacques and Hanson, Curtis A and Vajdic, Claire M and Schenk, Maryjean and Leis, Jose F and Brown, Kevin M and Rothman, Nathaniel and Vachon, Celine M and Low, Hui-Qi and Morton, Lindsay M and Spector, Logan G and Brennan, Paul and Weinberg, J Brice and Achenbach, Sara J and Skibola, Christine F and Armstrong, Bruce and Chanock, Stephen and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för onkologi, radiologi och klinisk immunologi and Uppsala universitet
Nature Genetics, ISSN 1061-4036, 08/2010, Volume 42, Issue 8, pp. 661 - 664
Journal Article