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Volumn 132, Issue 1, 2002, Pages 61-64

Fluorescence in situ hybridization analysis of the cryptic t(12;21) (p13;q22) in childhood B-lineage acute lymphoblastic leukemia

(7) Yehuda Gafni, Orly a Cividalli, Gabriel a Abrahmov, Ayala b Weintrob, Michael a Neriah, Susana Ben a Cohen, Rachel a Abeliovich, Dvorah a

a HADASSAH HEBREW UNIVERSITY MEDICAL CENTER (Israel)

b SHAARE ZEDEK MEDICAL CENTER (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE LYMPHOBLASTIC LEUKEMIA; ARTICLE; B LYMPHOCYTE; CELL LINEAGE; CHILD; CHILDHOOD LEUKEMIA; CHROMOSOME TRANSLOCATION 12; CHROMOSOME TRANSLOCATION 21; CLINICAL ARTICLE; CONTROLLED STUDY; CYTOGENETICS; DIPLOIDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FUSION GENE; GENE LOCUS; GENE PROBE; HUMAN; INTERPHASE; MALE; METAPHASE CHROMOSOME; MOLECULAR CLONING; PRIORITY JOURNAL;

CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 12; CHROMOSOMES, HUMAN, PAIR 21; CORE BINDING FACTOR ALPHA 2 SUBUNIT; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; LEUKEMIA, B-CELL, ACUTE; MALE; ONCOGENE PROTEINS, FUSION; RETROSPECTIVE STUDIES; TRANSLOCATION, GENETIC;

EID: 0036160351 PISSN: 01654608 EISSN: None Source Type: Journal
DOI: 10.1016/S0165-4608(01)00530-1 Document Type: Article

Times cited : (10)

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