Translocation (11;14) is a common cytogenetic abnormality in clonal plasma cells in monoclonal immunoglobulin deposition disease

Bhutani, D., Liu, Y., Chakraborty, R., Radhakrishnan, J., Lentzsch, S., Peters, D., & Rubinstein, S. (2024). Translocation (11;14) is a common cytogenetic abnormality in clonal plasma cells in monoclonal immunoglobulin deposition disease. British Journal of Haematology, 205(5), 1860–1865. Portico. https://doi.org/10.1111/bjh.19748
Authors:
Divaya Bhutani
Yusha Liu
Rajshekhar Chakraborty
Jai Radhakrishnan
Suzanne Lentzsch
Daniel Peters
Samuel Rubinstein
Affiliated Authors:
Divaya Bhutani
Rajshekhar Chakraborty
Jai Radhakrishnan
Suzanne Lentzsch
Columbia Affiliation:
Subjects:
Translocation, Genetic (MeSH)
Plasma Cells (MeSH)
Chromosomes, Human, Pair 14 (MeSH)
Author Keywords:
cytogenetics
light chain deposition disease
monoclonal immunoglobulin deposition disease
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Publication Type:
Article
Unique ID:
10.1111/bjh.19748
PMID:
39239804
DOI:
10.1111/bjh.19748
Journal:
British Journal of Haematology
Publication Date:
Data Source:
PubMed
Source Link:
View PubMed Record
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