Evidence of two different molecular mechanisms as a consequence of an isolated 20q- abnormality in a case of multiple myeloma accompanied with myelodysplastic syndrome-Reference-Cited by-同舟云学术

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Evidence of two different molecular mechanisms as a consequence of an isolated 20q- abnormality in a case of multiple myeloma accompanied with myelodysplastic syndrome

Published:2021 Issue: Volume:16 Page:100273
ISSN:2213-0489
Container-title:Leukemia Research Reports
language:en
Short-container-title:Leukemia Research Reports

Author:

Mitev Lubomir

Publisher

Elsevier BV

Subject

Oncology,Hematology

Reference13 articles.

1. del(20q) in myeloid malignancies;Bilhou-Nabera;Atlas Genet. Cytogenet. Onco. Haematol,2001

2. Clinical course of patients with incidental finding of 20q- in the bone marrow without a morphologic evidence of multiple myeloma;Jawad;Am. J. Hematol.,2016

3. Coexistance of multiple myeloma and myelodysplastic syndrome or lymphoid diseasesat diagnosis: evidence for two clonal and independent chromosome abnormalities;Mossafa;Blood,2011

4. Deletion(20q) as the sole abnormality in plasma cell myeloma is not associated with plasma cells as identified by clg FISH;White;Cancer Genet,2012

5. Isolated chromosome 20q deletions in patients with non-myeloid disorders;Andrea;Blood,2012

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hereditable variants of classical protein tyrosine phosphatase genes: Will they prove innocent or guilty?;Frontiers in Cell and Developmental Biology;2023-01-23

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