Chromosomes and causation of human cancer and leukemia. XVII. Banding studies in acute myeloblastic leukemia (AML)
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Summary
The present data suggest that some chromosomal changes are nonrandom in AML and that further chromosomal studies may lead to a division of AML patients into subgroups on the basis of their karyotypes.
- Type
- article
- Published
- 1976-08-01
- Cited by
- 108
- References
- 43
- OpenAlex
- https://openalex.org/W1989127893
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:40393517
Keywords
Karyotype, Acute myeloblastic leukemia, Chromosomal translocation, Trisomy, Leukemia
References
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- Tumor Etiology and Chromosome Pattern
- Chromosomes and causation of human cancer and leukemia. X Banding patterns in cancerous effusions
- Clinical implications of aneuploid cyto genetic profiles in adult acute leukemia
- An abnormal cell‐line in a patient with acute granulocytic leukemia. Cytogenetic studies before and after an allogeneic marrow transplant
- Trisomy‐9 in the Bone Marrow of a Patient with Acute Myelomonoblastic Leukaemia
- Acquired trisomy 9.
- Cytogenetic studies and their clinical correlates in adults with acute leukemia.
- Chromosomes and causation of human cancer and leukemia. V. Karyotypic aspects of acute leukemia
- 8‐trisomy in the bone marrow. Report of two cases
- Acquired trisomy 9.
- Cytologic studies of tumors XLVII. Acute myelogenous leukemia with C/G translocation and differential response to PHA of normal and leukemic cells of blood and marrow
- Acquired G‐group trisomy in acute monomyeloblastic leukemia
- CHROMOSOME CHANGES IN HUMAN LEUKEMIA AND A TENTATIVE ASSESSMENT OF THEIR SIGNIFICANCE
- The missing Y chromosome and human leukaemia.
Cited by
- Clinical implications of chromosome abnormalities in acute non-lymphocytic leukemia: Current status
- Cytogenetic patterns in acute nonlymphocytic leukemia
- Hairy cell leukemia: An analysis of the chromosomes of 26 patients
- Hematologic and cytologic characterization of 8/21 translocation acute granulocytic leukemia.
- Nonrandom abnormalities in chromosome 1 in human testicular cancers.
- The clinical significance of cytogenetic studies in 100 patients with multiple myeloma, plasma cell leukemia, or amyloidosis.
- Correlation of clinical findings with quinacrine-banded chromosomes in 90 adults with acute nonlymphocytic leukemia: an eight-year study (1970-1977).
- Emergence of a cell line with extreme hypodiploidy in blast crisis of chronic myelocytic leukemia.
- Cytogenetic and immunoglobulin markers of human leukemic B-cell lines.
- Nonrandom chromosome abnormalities in acute leukemia and dysmyelopoietic syndromes in patients with previously treated malignant disease.
- Nonrandom cytogenetic changes in human acute leukemia and their clinical implications.
- Cytogenetic studies in adult acute leukemias.
- Chromosomes and causation of human cancer and leukemia XXXV. The missing Y in acute non‐lymphocytic leukemia (ANLL)
- Duplication of part of chromosome no. 1 in myeloproliferative diseases.
- The 5q-anomaly.
- Lymphoblastic lymphoma in adults
- 14q+ marker chromosomes in multiple myeloma and plasma-cell leukaemia.
- Cytogenetics of childhood acute nonlymphocytic leukemia.
- Nonrandom cytogenetic changes in New Zealand patients with acute myeloid leukemia.
- Cytogenetic studies on acute monocytic leukemia.
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