Identification of variant translocations in chronic myeloid leukemia by fluorescence in situ hybridization
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference19 articles.
1. A new consistent chromosomal abnormality in chronic myelogenous leukemia identified by quinacrine fluorescence and Giemsa staining;Rowley;Nature,1973
2. The Chromosomes in Human Cancer and Leukemia;Sandberg,1991
3. Variant Philadelphia translocations in chronic myeloid leukemia;De Braekeloer;Cytogenet Cell Genet,1987
4. The Philadelphia chromosome. Consideration based on studies of variant translocation;Ishihara;Cancer Genet Cytogenet,1988
5. Cytogenetic and molecular studies in patients with chronic myeloid leukemia and variant Philadelphia translocations;Zaccara;Cancer Genet Cytogenet,1989
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1. Evaluation of cytogenetic response in CML patients with variant Philadelphia translocation;Asia-Pacific Journal of Clinical Oncology;2021-02-25
2. A Novel Four-Way Complex Variant Translocation Involving Chromosome 46,XY,t(4;9;19;22)(q25:q34;p13.3;q11.2) in a Chronic Myeloid Leukemia Patient;Frontiers in Oncology;2016-05-30
3. Variant Philadelphia translocations with different breakpoints in six chronic myeloid leukemia patients;Turkish Journal of Hematology;2011-08-01
4. Chronic Myelogenous Leukemia with a Variant Philadelphia Translocation: t(11;22)(q25;q11.2);Annals of Laboratory Medicine;2006-08-01
5. Complex chromosomal rearrangements in patients with chronic myeloid leukemia;Cancer Genetics and Cytogenetics;2006-07
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