TY  - GEN
AU  - Streubel,B
AU  - Vinatzer,U
AU  - Lamprecht,A
AU  - Raderer,M
AU  - Chott,A
TI  - T(3;14)(p14.1;q32) involving IGH and FOXP1 is a novel recurrent chromosomal aberration in MALT lymphoma
SN  - 0887-6924
PY  - 2005///0526
KW  - Adaptor Proteins, Signal Transducing
KW  - genetics
KW  - Aged
KW  - Aged, 80 and over
KW  - B-Cell CLL-Lymphoma 10 Protein
KW  - Caspases
KW  - Chromosomes, Human, Pair 14
KW  - Chromosomes, Human, Pair 3
KW  - Cloning, Molecular
KW  - Female
KW  - Forkhead Transcription Factors
KW  - Humans
KW  - Immunoglobulin Heavy Chains
KW  - In Situ Hybridization, Fluorescence
KW  - Lymphoma, B-Cell, Marginal Zone
KW  - Male
KW  - Middle Aged
KW  - Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein
KW  - Neoplasm Proteins
KW  - Repressor Proteins
KW  - Translocation, Genetic
KW  - Trisomy
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1038/sj.leu.2403644
ER  -