TY  - GEN
AU  - Licht,J D
AU  - Chomienne,C
AU  - Goy,A
AU  - Chen,A
AU  - Scott,A A
AU  - Head,D R
AU  - Michaux,J L
AU  - Wu,Y
AU  - DeBlasio,A
AU  - Miller,W H
TI  - Clinical and molecular characterization of a rare syndrome of acute promyelocytic leukemia associated with translocation (11;17)
SN  - 0006-4971
PY  - 1995///0316
KW  - Adult
KW  - Aged
KW  - Aged, 80 and over
KW  - Amino Acid Sequence
KW  - Antineoplastic Combined Chemotherapy Protocols
KW  - therapeutic use
KW  - Base Sequence
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 11
KW  - Chromosomes, Human, Pair 17
KW  - Cloning, Molecular
KW  - DNA Primers
KW  - DNA-Binding Proteins
KW  - genetics
KW  - Female
KW  - Humans
KW  - Kruppel-Like Transcription Factors
KW  - Leukemia, Promyelocytic, Acute
KW  - classification
KW  - Male
KW  - Middle Aged
KW  - Molecular Sequence Data
KW  - Polymerase Chain Reaction
KW  - Promyelocytic Leukemia Zinc Finger Protein
KW  - RNA, Messenger
KW  - analysis
KW  - Receptors, Retinoic Acid
KW  - Retinoic Acid Receptor alpha
KW  - Syndrome
KW  - Transcription Factors
KW  - Translocation, Genetic
KW  - Tretinoin
KW  - Zinc Fingers
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
ER  -