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Clinical and molecular characterization of a rare syndrome of acute promyelocytic leukemia associated with translocation (11;17).
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Clinical and molecular characterization of a rare syndrome of acute promyelocytic leukemia associated with translocation (11;17).
Clinical and molecular characterization of a rare syndrome of acute promyelocytic leukemia associated with translocation (11;17). Blood. 1995 Feb 15; 85(4):1083-94.
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PubMed
subject areas
Adult
Aged
Aged, 80 and over
Amino Acid Sequence
Antineoplastic Combined Chemotherapy Protocols
Base Sequence
Chromosome Mapping
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 17
Cloning, Molecular
DNA Primers
DNA-Binding Proteins
Female
Humans
Kruppel-Like Transcription Factors
Leukemia, Promyelocytic, Acute
Male
Middle Aged
Molecular Sequence Data
Polymerase Chain Reaction
Promyelocytic Leukemia Zinc Finger Protein
Receptors, Retinoic Acid
Retinoic Acid Receptor alpha
RNA, Messenger
Syndrome
Transcription Factors
Translocation, Genetic
Tretinoin
Zinc Fingers
authors with profiles
HAGOP M KANTARJIAN
JORGE E CORTES