FISH and SNP-A karyotyping in myelodysplastic syndromes: improving cytogenetic detection of del(5q), monosomy 7, del(7q), trisomy 8 and del(20q).
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L. Gondek | J. Maciejewski | M. Sekeres | H. Makishima | J. Huh | K. Theil | J. Cook | E. Kuczkowski | Manjot Rataul | C. O’Keefe
[1] Jungwon Huh,et al. Loss of heterozygosity 4q24 and TET2 mutations associated with myelodysplastic/myeloproliferative neoplasms. , 2009, Blood.
[2] G. Mufti,et al. Whole genome scanning as a cytogenetic tool in hematologic malignancies. , 2008, Blood.
[3] C. O'keefe,et al. Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML. , 2008, Blood.
[4] C. Evers,et al. Molecular definition of chromosome arm 5q deletion end points and detection of hidden aberrations in patients with myelodysplastic syndromes and isolated del(5q) using oligonucleotide array CGH , 2007, Genes, chromosomes & cancer.
[5] C. O'keefe,et al. Clonality of the stem cell compartment during evolution of myelodysplastic syndromes and other bone marrow failure syndromes , 2007, Leukemia.
[6] Å. Borg,et al. High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration , 2006, Leukemia.
[7] M. Mancini,et al. Detection and monitoring of trisomy 8 by fluorescence in situ hybridization in acute myeloid leukemia: a multicentric study. , 1998, Haematologica.
[8] T Hamblin,et al. International scoring system for evaluating prognosis in myelodysplastic syndromes. , 1997, Blood.
[9] C. Preudhomme,et al. Fluorescence in situ hybridization improves the detection of monosomy 7 in myelodysplastic syndromes. , 1994, Leukemia.
[10] A. Duhamel,et al. Cytogenetic analysis has strong independent prognostic value in de novo myelodysplastic syndromes and can be incorporated in a new scoring system: a report on 408 cases. , 1993, Leukemia.
[11] D J Schaid,et al. Fluorescence in situ hybridization: a sensitive method for trisomy 8 detection in bone marrow specimens. , 1992, Blood.
[12] G. Mufti. Chromosomal deletions in the myelodysplastic syndrome. , 1992, Leukemia research.
[13] Iscn. International System for Human Cytogenetic Nomenclature , 1978 .