Trisomy of chromosome 22 in acute myelomonocytic leukemia
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference13 articles.
1. Identification of a translocation with quinacrine fluorescence in a patient with acute leukemia;Rowley;Ann Genet,1973
2. 1517 Translocation, a consistant chromosomal change in acute promyelocytic leukemia;Rowley;Lancet,1977
3. Acute monocytic leukemia chromosome studies;Berger;Leuk Res,1982
4. Translocation (9;11) (p21;q23) in three cases of acute monoblastic leukemia;Hagemeyer;Cancer Genet Cytogenet,1982
5. Association of an inversion of chromosome 16 with abnormal marrow eosinophils in acute myelomonocytic leukemia: A unique cytogenetic-clinic-pathological association;Lebeau;N Engl J Med,1983
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3. Trisomy 22 as the Sole Abnormality is an Important Marker for the Diagnosis of Acute Myeloid Leukemia with Inversion 16;Onkologie;2008
4. Concurrent acute myeloid leukemia with inv(16)(p13.1q22) and chronic lymphocytic leukemia: Molecular evidence of two separate diseases;American Journal of Hematology;2006-12
5. Trisomy 22 as the Sole Karyotypic Abnormality in Myelodysplastic Syndrome;International Journal of Hematology;2005-04-01
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