Ranni N S, Slavutsky I, Wechsler A, Brieux de Salum S
Cancer Genet Cytogenet. 1987 Apr;25(2):309-16. doi: 10.1016/0165-4608(87)90192-0.
Cytogenetic studies were performed on six patients with multiple myeloma in which G-banding allowed the identification of clonal chromosome abnormalities. Normal cells and random chromosome gains and losses were seen in all cases. Numerical clonal aberrations were observed in two cases. Among the remaining cases, clonal chromosome rearrangements were seen in two cases, whereas, the other two patients revealed both numerical and structural clonal anomalies. The following marker chromosomes were identified: 1q-, 2p+, 2q+, 7q-, 17p-, and five unidentified abnormal chromosomes.
对6例多发性骨髓瘤患者进行了细胞遗传学研究,通过G显带可识别克隆性染色体异常。所有病例均可见正常细胞以及随机的染色体增减。2例观察到数值性克隆畸变。在其余病例中,2例可见克隆性染色体重排,而另外2例患者同时存在数值性和结构性克隆异常。识别出以下标记染色体:1q-、2p+、2q+、7q-、17p-,以及5条未识别的异常染色体。