Genomic characterization of the chromosomal breakpoints of t(4;14) of multiple myeloma suggests more than one possible aetiological mechanism. [electronic resource]
Producer: 20030314Description: 1103-13 p. digitalISSN:- 0950-9232
- B-Lymphocytes -- pathology
- Base Sequence
- Cell Transformation, Neoplastic -- genetics
- Chromosome Breakage
- Chromosomes, Human, Pair 14 -- genetics
- Chromosomes, Human, Pair 4 -- genetics
- Clone Cells -- pathology
- Gene Rearrangement, B-Lymphocyte, Heavy Chain
- Genes, Immunoglobulin
- Genes, Switch
- Humans
- Immunoglobulin Class Switching -- genetics
- Immunoglobulin Switch Region -- genetics
- Immunoglobulin mu-Chains -- genetics
- Models, Biological
- Molecular Sequence Data
- Multiple Myeloma -- etiology
- Neoplastic Stem Cells -- pathology
- Polymerase Chain Reaction -- methods
- Sequence Alignment
- Sequence Homology, Nucleic Acid
- Translocation, Genetic -- genetics
No physical items for this record
Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.