Refractory anemia with ring sideroblasts associated with i(17q) and mutation of the TP53 gene

Cancer Genetics and Cytogenetics

Volumn 136, Issue 1, 2002, Pages 86-89

  Lazarevi, Vladimir ^a   Djordjevi, Vesna ^a   Magi, Zvonko ^b   Marisavljevic, Dragomir ^a   Olovi, Milica ^a  

^a CLINICAL CENTER OF SERBIA   (Serbia)

^b UNIVERSITY OF DEFENCE   (Serbia)

Author keywords

[No Author keywords available]

Indexed keywords

DANAZOL; PYRIDOXINE;

AGED; ARTICLE; BONE MARROW BIOPSY; CASE REPORT; CHROMOSOME 17Q; CHROMOSOME ABERRATION; CLINICAL FEATURE; CYTOGENETICS; DISEASE COURSE; DISEASE SEVERITY; ERYTHROCYTE TRANSFUSION; EXON; GENE MUTATION; HUMAN; HUMAN CELL; ISOCHROMOSOME; MALE; METAPHASE CHROMOSOME; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL; REFRACTORY ANEMIA; SIDEROBLASTIC ANEMIA; SINGLE STRAND CONFORMATION POLYMORPHISM; THROMBOCYTE TRANSFUSION;

EID: 0036649147     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(02)00510-1     Document Type: Article

References (9)

1. FAB cooperative group. Proposals for the classification of the myelodysplastic syndromes
2. Isochromosomes in neoplasia
3. Myelodysplastic syndrome and acute myeloid leukemia with 17p deletion: An entity characterized by specific dysgranulopoiesis and high incidence of P53 mutations
4. Isolated isochromosome 17q: A distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical course
5. Erythroid colony formation in cultures of mouse and human bone marrow: Analysis of the requirements of erythropoietin by gel filtration and affinity chromatography on agarose-concavalin
6. Rapid method for obtaining high quality chromosome banding in the study of hematopoietic neoplasia
7. Detection of polymorphism of human DNA by gel electrophoresis as single strand conformation polymorphisms
8. Two types of acquired sideroblastic anemia (AISA)
9. Isochromosome 17q in blast crisis of chronic myeloid leukemia and in other hematologic malignanicies is the result of clustered breakpoints in 17p11 and is not associated with coding TP53 mutations