A unique, complex variant Philadelphia chromosome translocation in a patient with typical chronic myelogenous leukemia

Archives of Pathology and Laboratory Medicine

Volumn 125, Issue 3, 2001, Pages 437-439

  Oudat, R ^a   Khan, Z ^a   Glassman, A B ^a  

^a Dept Hematopathol Clin Cytogen ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BONE MARROW BIOPSY; CASE REPORT; CHROMOSOME 11P; CHROMOSOME 22Q; CHROMOSOME 9; CHROMOSOME G BAND; CHROMOSOME TRANSLOCATION; CHRONIC MYELOID LEUKEMIA; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN TISSUE; MALE; PHILADELPHIA 1 CHROMOSOME;

ADULT; ANTINEOPLASTIC AGENTS; CHROMOSOME PAINTING; HUMANS; HYDROXYUREA; KARYOTYPING; LEUKEMIA, MYELOID, CHRONIC; MALE; PHILADELPHIA CHROMOSOME; TRANSLOCATION, GENETIC;

EID: 0035094405     PISSN: 00039985     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (9)

1. A minute chromosome in human granulocytic leukemia
2. A new consistent chromosomal abnormality in chronic myelogenous leukemia identified by quinacrine fluorescence and Giemsa staining
3. A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukemia
4. Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22
5. bcr-abl RNA in patients with chronic myelogenous leukemia
6. Cytogenetic peculiarities in chronic myelogenous leukemia
7. Prognostic study of alpha-interferon (INF)-treated chronic myelogenous leukemia (CML) patients: II. Predicting survival
8. White cells, lymph node and spleen