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Volumn 134, Issue 1, 2002, Pages 55-59

New cytogenetic variant, insertion (15;17)(q22;q12q21), in an adolescent with acute promyelocytic leukemia

(6) Rolston, Raj a Weck, Karen E a Tersak, Jean M a,b Sherer, Maureen E c,d Cumbie, Kathleen d Shekhter Levin, Sofia c,d,e

a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE (United States)

b CHILDREN S HOSPITAL OF PITTSBURGH (United States)

c UNIVERSITY OF PITTSBURGH (United States)

d UNIVERSITY OF PITTSBURGH (United States)

e UNIVERSITY OF PITTSBURGH CANCER INSTITUTE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CHROMOSOME 15; CHROMOSOME 17; CHROMOSOME IDENTIFICATION; CHROMOSOME REARRANGEMENT; CYTOGENETICS; DNA PROBE; FEMALE; FLUORESCENCE; FUSION GENE; GENE FUSION; GENE IDENTIFICATION; GENE INSERTION; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; HUMAN; IN SITU HYBRIDIZATION; INTRON; PRIORITY JOURNAL; PROMYELOCYTIC LEUKEMIA; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

ADOLESCENT; CHROMOSOMES, HUMAN, PAIR 15; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; LEUKEMIA, PROMYELOCYTIC, ACUTE; TRANSLOCATION, GENETIC;

INSERTION SEQUENCES;

EID: 0036538824 PISSN: 01654608 EISSN: None Source Type: Journal
DOI: 10.1016/S0165-4608(01)00595-7 Document Type: Article

Times cited : (6)

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