General population low-count CLL-like MBL persists over time without clinical progression, although carrying the same cytogenetic abnormalities of CLL. [electronic resource]
Producer: 20120316Description: 6618-25 p. digitalISSN:- 1528-0020
- Adult
- Aged
- Aged, 80 and over
- B-Lymphocytes -- metabolism
- Chromosome Aberrations
- Chromosomes, Human, Pair 12 -- genetics
- Chromosomes, Human, Pair 13 -- genetics
- Chromosomes, Human, Pair 17 -- genetics
- Disease Progression
- Female
- Flow Cytometry
- Follow-Up Studies
- Humans
- In Situ Hybridization, Fluorescence
- Leukemia, Lymphocytic, Chronic, B-Cell -- diagnosis
- Lymphocyte Count
- Lymphocytosis -- diagnosis
- Male
- Middle Aged
- Receptors, Antigen, T-Cell, alpha-beta -- metabolism
- T-Lymphocytes -- metabolism
- V(D)J Recombination -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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