5'RARA submicroscopic deletion from new variant translocation involving chromosomes 15, 17, and 18, in a case of acute promyelocytic leukemia. [electronic resource]
Producer: 20080422Description: 50-5 p. digitalISSN:- 0165-4608
- Chromosomes, Human, Pair 15
- Chromosomes, Human, Pair 17
- Chromosomes, Human, Pair 18
- Female
- Humans
- In Situ Hybridization, Fluorescence
- Karyotyping
- Leukemia, Promyelocytic, Acute -- genetics
- Middle Aged
- Receptors, Retinoic Acid -- genetics
- Retinoic Acid Receptor alpha
- Sequence Deletion
- Translocation, Genetic
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Publication Type: Case Reports; Journal Article
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