A new reliable fluorescence in situ hybridization method for identifying multiple specific cytogenetic abnormalities in acute myeloid leukemia. [electronic resource]
Producer: 20100806Description: 680-5 p. digitalISSN:- 1029-2403
- Chromosome Aberrations
- Chromosome Inversion
- Chromosomes, Human, Pair 15
- Chromosomes, Human, Pair 16
- Chromosomes, Human, Pair 7
- DNA Mutational Analysis -- methods
- Female
- Histone-Lysine N-Methyltransferase
- Humans
- In Situ Hybridization, Fluorescence -- methods
- Leukemia, Myeloid, Acute -- genetics
- Male
- Models, Biological
- Monosomy
- Myeloid-Lymphoid Leukemia Protein -- genetics
- Oncogene Proteins, Fusion -- analysis
- Reproducibility of Results
- Substrate Specificity -- genetics
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Publication Type: Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't
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