Tetrasomy 21 as the sole acquired karyotypic abnormality in acute myeloblastic leukemia

Cancer Genetics and Cytogenetics

Volumn 128, Issue 2, 2001, Pages 158-160

  Odagaki, Takao ^a   Sugimoto, Takeshi ^a   Matsuo, Mari ^a   Tatsumi, Eiji ^b   Saigo, Katsuyasu ^a,c  

^a Kobe Kyodo Hospital   (Japan)

^b KOBE UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c KOBE UNIVERSITY HOSPITAL   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CYTARABINE;

ACUTE MYELOBLASTIC LEUKEMIA; AGED; ARTICLE; BLOOD ANALYSIS; BONE MARROW EXAMINATION; CASE REPORT; CELL DIFFERENTIATION; CHROMOSOME ABERRATION; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE COURSE; FEMALE; HUMAN; HUMAN CELL; KARYOTYPE; KARYOTYPING; PRIORITY JOURNAL; TETRASOMY;

AGED; BONE MARROW; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 21; FEMALE; HUMANS; KARYOTYPING; LEUKEMIA, MYELOCYTIC, ACUTE;

EID: 0035878532     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(01)00408-3     Document Type: Article

References (19)

1. Numerical chromosome aberration in human neoplasia
2. Heterogeneity of hyperdiploid (51-67) childhood acute lymphoblastic leukemia
3. Clinical and prognostic significance of trisomy 21 in adult patients with acute myelogenous leukemia and myelodysplastic syndromes
4. Trisomy 21 in acute myeloid leukemia
5. Randomized study of individualized induction therapy with or without vincristine, and of maintenance-intensification therapy between 4 or 12 courses in adult acute leukemia
6. The mortality from leukaemia and other cancers among patients with Down's syndrome (Mongols) and among their parents
7. Acute lymphoblastic leukemia and chromosome
8. Cytogenetics of acutely transformed chronic myeloproliferative syndromes without a Philadelphia chromosome
9. Transient myeloproliferative syndrome disorder (TMD) with transiently increased tetrasomy-21 cells in a phenotypically normal newborn
10. Hematologic disorders in 13 patients with acquired trisomy 21 and 13 individuals with Down syndrome
11. Tetrasomy 21 in megakaryoblastic leukemia
12. Tetrasomy 21 as a sole abnormality in erythroleukemia
13. Chronic neutrophil leukaemia in adolescence and young adulthood
14. Trisomy 21 as the sole acquired karyotypic abnormality in acute myeloid leukemia and myelodysplastic syndrome
15. Down syndrome and chromosome 21 abnormalities in leukemia
16. ETS family of genes in leukemia and Down syndrome
17. Increased levels of a chromosome 21-encoded tumour invasion and metastasis factor (TIAM1) mRNA in bone marrow of Down syndrome children during acute phase of AML (M7)
18. Disomic homozygosity in 21-trisomic cells: A mechanism responsible for transient myeloproliferative syndrome
19. Possible mapping of the gene for transient myeloproliferative syndrome at 21q11.2