Primary myelodysplastic syndrome with normal cytogenetics: Utility of ‘FISH panel testing’ and M-FISH

Leukemia Research

Volumn 26, Issue 3, 2002, Pages 235-240

  Ketterling, Rhett P ^a   Wyatt, William A ^a   VanWier, Scott A ^a   Law, Mark ^a   Hodnefield, Janice M ^a   Hanson, Curtis A ^a   Dewald, Gordon W ^a  

^a MAYO CLINIC   (United States)

Author keywords

Chromosome; Cytogenetics; FISH; Hematology; M FISH; Myelodysplastic syndrome

Indexed keywords

ADULT; AGED; ARTICLE; CELL CYCLE; CHROMOSOME 13Q; CHROMOSOME ABERRATION; CHROMOSOME DELETION 13; CHRONIC MYELOID LEUKEMIA; CLINICAL ARTICLE; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; CYTOGENETICS; DOUBLE BLIND PROCEDURE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN TISSUE; INTERMETHOD COMPARISON; INTERPHASE; KARYOTYPE; MALE; METAPHASE; MYELODYSPLASTIC SYNDROME; PRELEUKEMIA; PRIORITY JOURNAL; PROGNOSIS; RANDOMIZED CONTROLLED TRIAL; TECHNIQUE;

ANEMIA, REFRACTORY, WITH EXCESS OF BLASTS; BONE MARROW CELLS; CELL NUCLEUS; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 13; HEMATOLOGIC DISEASES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INTERPHASE; KARYOTYPING; METAPHASE; MONOSOMY; MYELODYSPLASTIC SYNDROMES; OBSERVER VARIATION; REFERENCE VALUES; TRISOMY;

EID: 17044453376     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0145-2126(01)00117-5     Document Type: Article

References (13)

1. Epidemiological and etiological aspects of myelodysplastic syndromes
2. Diagnosis, classification, and cytogenetics of myelodysplastic syndromes
3. Cytogenetics of myelodysplastic syndromes
4. Molecular features of primary MDS with cytogenetic changes
5. Molecular genetic features of myelodysplastic syndromes (MDS)
6. Dynamics of chromosome spreading
7. M-FISH technique: how to set up and analyze
8. Efficacy of fluorescence in situ hybridization for detecting PML/RARA gene fusion in treated and untreated acute promyelocytic leukemia
9. Review of clinical, cytogenetic and molecular aspects of Ph-negative CML
10. Detection of t(12;21) in childhood acute lymphoblastic leukemia by fluorescence in situ hybridization
11. Diagnostic and prognostic significance of cytogenetics in adult primary myelodysplastic syndromes
12. Detection of RB1 deletions by fluorescence in situ hybridization in malignant hematologic disorders
13. Utility of multicolor fluorescent in situ hybridization in clinical cytogenetics