The t(15;17) breakpoint in acute promyelocytic leukemia cluster within two different sites of the myl gene: targets for the detection of minimal residual disease by the polymerase chain reaction. [electronic resource]
Producer: 19920227Description: 554-8 p. digitalISSN:- 0006-4971
- Base Sequence
- Blotting, Northern
- Carrier Proteins -- genetics
- Chromosome Aberrations -- diagnosis
- Chromosome Disorders
- Chromosomes, Human, Pair 15
- Chromosomes, Human, Pair 17
- Humans
- Leukemia, Promyelocytic, Acute -- diagnosis
- Molecular Sequence Data
- Oligonucleotides -- chemistry
- Polymerase Chain Reaction
- RNA, Messenger -- genetics
- Receptors, Retinoic Acid
- Translocation, Genetic -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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