Niss R, Passarge E
J Med Genet. 1976 Jun;13(3):229-34. doi: 10.1136/jmg.13.3.229.
In the course of re-examing cultured fibroblasts stored in liquid nitrogen from a patient with developmental retardation, solitary left kidney, and Wilms tumour, a cell line trisomic for chromosome 8 was found. Trisomy 8 was restricted to fibroblasts in the first 22 subcultures and was absent in later passages as well as in lymphocytes. A familial pericentric inversion of chromosome 2 was observed in three generations including the propositus but was though to be unrelated to the clinical problem. Multiple spontaneous chromosomal rearrangements were seen in several late subcultures.
在重新检查一名患有发育迟缓、孤立性左肾和肾母细胞瘤患者储存在液氮中的培养成纤维细胞过程中,发现了一个8号染色体三体的细胞系。8号染色体三体在前22代传代培养的成纤维细胞中存在,而在后续传代以及淋巴细胞中不存在。在包括先证者在内的三代人中观察到2号染色体的家族性臂间倒位,但认为与临床问题无关。在几个后期传代培养物中发现了多个自发染色体重排。