T(3;14)(p14.1;q32) involving IGH and FOXP1 is a novel recurrent chromosomal aberration in MALT lymphoma.
Streubel, B
T(3;14)(p14.1;q32) involving IGH and FOXP1 is a novel recurrent chromosomal aberration in MALT lymphoma. [electronic resource] - Leukemia Apr 2005 - 652-8 p. digital
Publication Type: Journal Article
0887-6924
10.1038/sj.leu.2403644 doi
Adaptor Proteins, Signal Transducing--genetics
Aged
Aged, 80 and over
B-Cell CLL-Lymphoma 10 Protein
Caspases
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 3
Cloning, Molecular
Female
Forkhead Transcription Factors
Humans
Immunoglobulin Heavy Chains--genetics
In Situ Hybridization, Fluorescence
Lymphoma, B-Cell, Marginal Zone--genetics
Male
Middle Aged
Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein
Neoplasm Proteins--genetics
Repressor Proteins--genetics
Translocation, Genetic
Trisomy
T(3;14)(p14.1;q32) involving IGH and FOXP1 is a novel recurrent chromosomal aberration in MALT lymphoma. [electronic resource] - Leukemia Apr 2005 - 652-8 p. digital
Publication Type: Journal Article
0887-6924
10.1038/sj.leu.2403644 doi
Adaptor Proteins, Signal Transducing--genetics
Aged
Aged, 80 and over
B-Cell CLL-Lymphoma 10 Protein
Caspases
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 3
Cloning, Molecular
Female
Forkhead Transcription Factors
Humans
Immunoglobulin Heavy Chains--genetics
In Situ Hybridization, Fluorescence
Lymphoma, B-Cell, Marginal Zone--genetics
Male
Middle Aged
Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein
Neoplasm Proteins--genetics
Repressor Proteins--genetics
Translocation, Genetic
Trisomy