Secondary chromosome changes in mantle cell lymphoma: Cytogenetic and fluorescence in situ hybridization studies

Leukemia and Lymphoma

Volumn 40, Issue 5-6, 2001, Pages 581-590

  Bigoni, R ^a   Cuneo, A ^a   Milani, R ^a   Roberti, M G ^a   Bardi, A ^a   Rigolin, G M ^a   Cavazzini, F ^a   Agostini, P ^a   Castoldi, G ^a  

^a UNIVERSITY OF FERRARA   (Italy)

Author keywords

6Q21 deletion; 9P21 deletion; Chromosomes; Mantle cell lymphoma

Indexed keywords

PROTEIN P53;

ARTICLE; B CELL LYMPHOMA; BLAST CELL; CANCER GRADING; CHROMOSOME 10Q; CHROMOSOME 11Q; CHROMOSOME 12; CHROMOSOME 13Q; CHROMOSOME 17P; CHROMOSOME 1P; CHROMOSOME 20; CHROMOSOME 21; CHROMOSOME 22; CHROMOSOME 3Q; CHROMOSOME 6Q; CHROMOSOME 8P; CHROMOSOME 9P; CHROMOSOME 9Q; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; CHROMOSOME TRANSLOCATION 11; CHROMOSOME TRANSLOCATION 14; CLINICAL ARTICLE; CONTROLLED STUDY; CYTOGENETICS; DISEASE ASSOCIATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE PROBE; GENETIC ANALYSIS; HISTOPATHOLOGY; HUMAN; INCIDENCE; KARYOTYPE; MALE; MANTLE CELL LYMPHOMA; PRIORITY JOURNAL; PROTO ONCOGENE; X CHROMOSOME;

EID: 0035048745     PISSN: 10428194     EISSN: None     Source Type: Journal    
DOI: 10.3109/10428190109097656     Document Type: Article

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