2006•Cancer Genetics and CytogeneticsRequires access

Identification of 13q deletion, trisomy 1q, and IgH rearrangement as the most frequent chromosomal changes found in Korean patients with multiple myeloma

Soo‐Mee Bang, Young Ree Kim, Yunjung Cho, Hyun Sook, Eul‐Ju Seo, Chan Jeoung Park, Soo Jin Yoo, Hee Chan Kim, Honggu Chun, Hyun Chung Min, Bo Ra Oh, Tae Young Kim, Jae Hoon Lee, Dong Soon Lee

Open publisher page 39 citations

Abstract

This record does not include an abstract. Use the full-text link above if available.

About this research paper

What this paper is about

An abstract is not available in the OpenAlex record for this paper.

Why it matters

OpenAlex reports 39 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Key concepts: Biology, Chromosomal translocation, Trisomy, Chromosome 13, Fluorescence in situ hybridization, Karyotype, Multiple myeloma, Gene rearrangement