Conventional Karyotyping and Fluorescence In Situ Hybridization for Detection of Chromosomal Abnormalities in Multiple Myeloma

BACKGROUND: Multiple myeloma (MM) is a genetically heterogeneous disease, with cytogenetic findings that determine disease behavior. Genetic abnormalities can be assessed by fluorescence in situ hybridization (FISH) analysis and/or G-banded karyotyping. The two methods produce unique and overlapping...

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Detalles Bibliográficos
Autores principales: Crabtree, Matthew, Cai, Jennifer, Qing, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9275438/
https://www.ncbi.nlm.nih.gov/pubmed/35837374
http://dx.doi.org/10.14740/jh1007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9275438/
https://www.ncbi.nlm.nih.gov/pubmed/35837374
http://dx.doi.org/10.14740/jh1007

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