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Leukemia Research
Volume 26, Issue 11
, Pages 993-996
, November 2002
Comparison of cytogenetics with FISH in 40 myelodysplastic syndrome patients
References
- (FAB cooperative group)—Proposals for classification of the myelodysplastic syndrome. Br. J. Haematol. 1982;51:189–199
- World health organization classification of neoplastic diseases of the hematopoietic, World health organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: report of the clinical advisory committe meeting—Airlie House, Virginia, November 1997. J. Clin. Oncol. 1999;17(12):3835–3849
-
.
Cytogenetics of myelodysplastic syndromes.
Semin. Haemotol. 1996;33(2):127–138
- . Clonal cell lineage involvement in myelodysplastic syndrome studied by fluorescence in situ hybridization and morphology. Leukemia. 1996;10:662–668
- . Cytogenetic clonality in myelodysplastic syndrome studied with fluorescence in situ hybridization: lineage, response to growth factor therapy, and clone expansion. Blood. 1993;81(6):1580–1585
- International scoring system for evaluating prognosis in myelodysplastic syndrome. Blood. 1997;89(6):2079–2088
-
.
Current state of fluorescence in situ hybridization (FISH) in diagnostic pathology.
Cell Vision. 1997;4(7):16–31
- . Fluorescence in situ hybridization. Uses and limitations. Semin. Hematol. 2000;37(4):320–333
- Fluorescence in situ hybridization: a sensitive method for trisomy 8 detection in bone marrow specimens. Blood. 1992;79(12):3307–3315
- . Comparison between interphase and metaphase cytogenetics in detecting chromosome defects in hematological neoplasias. Am. J. Hematol. 1993;43:205–211
- Detection of monosomy 7 and trisomy 8 in myeloid neoplasia: a comparison of banding and fluorescence in situ hybridation. Blood. 1993;82(3):904–913
-
Tanaka K, Arif M, Eguchi M, Shintani MM, Kumaravel T.S., Asaoku H, et al. Interphase flurescence in situ hybridization overcomes pitfalls of G-banding analysis with special references to underestimation of chromomal aberration rates, Cancer Genet Cytogenet 1999;115:32–8.
-
Schröck E, Padilla-Nash H. Spectral karyotyping and multicolor fluorescence in situ hybridization reveal new tumor-specific chromosomal aberration. Semin. Hematol 2000;37(4):334–47.
- Quantitation of minimal residual disease in acute myelogenous leukemia and myelodysplastic syndrome in complete remission by molecular cytogenetics of progenitor cells. Leukemia. 1999;13:568–577
- . Acute promyelocytic leukemia: the sutdy of t(15;17) translocation by FISH, RT-PCR and cytogenetic techniques. Braz. J. Med. Biol. Res. 2001;34(6):735–743
-
F. Mitelman, editor. ISCN: An international system for human cytogenetic nomenclature. Basel: S. Karger, 1995.
- Fluorescence in situ hybridization analysis of t(3;12)(q26;q13): a recurring chromosomal abnormality involving the TEL gene (ETV6) in myelodysplastic synrome. Blood. 1996;88(2):682–689
- . Clonal karyotype abnormalities and clinical progress in the myelodysplastic syndrome. Br. J. Haematol. 1990;76:194–202
- . Hematological malignancies with a deletion of 11q23: cytogenetic and clinical aspects. Leukemia. 1998;12:823–827
PII: S0145-2126(02)00047-4
© 2002 Elsevier Science Ltd. All rights reserved.
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Leukemia Research
Volume 26, Issue 11
, Pages 993-996
, November 2002
