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Genes, Chromosomes & Cancer|December 4, 2002
Delineation of the minimal region of loss at 13q14 in multiple myelomaManal O Elnenaei, Rifat A Hamoudi, John Swansbury, et al.
Haematologica|August 18, 2012
CLLU1 expression has prognostic value in chronic lymphocytic leukemia after first-line therapy in younger patients and in those with mutated IGHV genesDavid Gonzalez, Monica Else, Dorte Wren, et al.
Cancer|September 22, 2007
The role of rituximab in combination with pentostatin or cladribine for the treatment of recurrent/refractory hairy cell leukemiaMonica Else, Nnenna Osuji, Francesco Forconi, et al.
Blood|May 16, 2002
Relationship between glutathione S-transferase M1, T1, and P1 polymorphisms and chronic lymphocytic leukemiaMartin Yuille, Alison Condie, Chantelle Hudson, et al.
Blood|September 28, 2011
Alemtuzumab therapy in T-cell prolymphocytic leukemia: comparing efficacy in a series treated intravenously and a study piloting the subcutaneous routeClaire E Dearden, Amit Khot, Monica Else, et al.
Leukemia & Lymphoma|December 11, 2007
Birth order pattern in the inheritance of chronic lymphocytic leukaemia and related lymphoproliferative diseaseViggo Jønsson, Geir Tjønnfjord, Sven Ove Samuelsen, et al.
The Hematology Journal : the Official Journal of the European Haematology Association|March 30, 2004
CD38 expression as a prognostic indicator in chronic lymphocytic leukaemiaPatrick D Thornton, Cristina Fernandez, Giada M Giustolisi, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|September 21, 2006
Folate metabolism polymorphisms influence risk of colorectal adenoma recurrenceRichard A Hubner, Kenneth R Muir, Jo-Fen Liu, et al.
Genes, Chromosomes & Cancer|July 30, 2013
The silent mutational landscape of infant MLL-AF4 pro-B acute lymphoblastic leukemiaSara E Dobbins, Amy L Sherborne, Yussanne P Ma, et al.
Leukemia Research|September 6, 2011
Role of 657del5 NBN mutation and 7p12.2 (IKZF1), 9p21 (CDKN2A), 10q21.2 (ARID5B) and 14q11.2 (CEBPE) variation and risk of childhood ALL in the Polish populationAgata Pastorczak, Patryk Górniak, Amy Sherborne, et al.
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