Clinical and molecular characterization of a rare syndrome of acute promyelocytic leukemia associated with translocation (11;17). [electronic resource]
Producer: 19950316Description: 1083-94 p. digitalISSN:- 0006-4971
- Adult
- Aged
- Aged, 80 and over
- Amino Acid Sequence
- Antineoplastic Combined Chemotherapy Protocols -- therapeutic use
- Base Sequence
- Chromosome Mapping
- Chromosomes, Human, Pair 11
- Chromosomes, Human, Pair 17
- Cloning, Molecular
- DNA Primers
- DNA-Binding Proteins -- genetics
- Female
- Humans
- Kruppel-Like Transcription Factors
- Leukemia, Promyelocytic, Acute -- classification
- Male
- Middle Aged
- Molecular Sequence Data
- Polymerase Chain Reaction
- Promyelocytic Leukemia Zinc Finger Protein
- RNA, Messenger -- analysis
- Receptors, Retinoic Acid -- genetics
- Retinoic Acid Receptor alpha
- Syndrome
- Transcription Factors -- genetics
- Translocation, Genetic
- Tretinoin -- therapeutic use
- Zinc Fingers -- genetics
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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