Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping

Haematologica

Volumn 85, Issue 11, 2000, Pages 1219-1221

  Calabrese, G ^a   Fantasia, D ^a   Spadano, A ^a   Morizio, E ^a   Di Bartolomeo, P ^a   Palka, G ^a  

^a NONE   (Italy)

Author keywords

AML; Chromosome changes; FISH; SKY

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADULT; AGED; ARTICLE; CHROMOSOME REARRANGEMENT; CLINICAL ARTICLE; CYTOGENETICS; DISEASE COURSE; FEMALE; HUMAN; KARYOTYPE; MALE; PROGNOSIS;

ACUTE DISEASE; ADULT; AGED; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 5; CHROMOSOMES, HUMAN, PAIR 8; DNA PROBES; FEMALE; FLUORESCENT DYES; HUMANS; KARYOTYPING; LEUKEMIA, MYELOID; MALE; MIDDLE AGED; PROGNOSIS;

EID: 0033658261     PISSN: 03906078     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (10)

1. The role of chromosome translocations in leukemogenesis
2. Complex chromosome translocation of standard t(8;21) and t(15;17) arise from a two-step mechanism as evidenced by fluorescence in situ hybridization analysis
3. Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping
4. Combined spectral karyotyping and DAPI banding analysis of chromosome abnormalities in myelodysplastic syndrome
5. Fusion of PDGF receptor beta to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation
6. Self fusion of the ALL-1 gene: A new genetic mechanism for acute leukemia
7. The unexplored 5q13 locus: A role in hematopoietic malignancies
8. Pentasomy 8q in myelodysplasia
9. p53 loss and point mutations are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis
10. Identification and chromosomal localisation by fluorescence in situ hybridisation of human gene of phosphoinositide-specific phospholipase C beta(1)