Watt J L, King D J, Palmer J B, Davidson R J
Cancer Genet Cytogenet. 1983 Jun;9(2):113-8. doi: 10.1016/0165-4608(83)90031-6.
A patient presenting with an unusual case of refactory anemia is described in whom acquired markers originating from chromosomes No. 5 and 8 are identified by G- and sequential C-banding. Comparison with various published illustrations of chromosome No. 5 deletions in this general broad category of disease raises the possibility that karyotypic misclassification in cases of absent or substandard banding (typical of bone marrow) may help to explain the considerable variation in size and morphology of the 5q--marker.
本文描述了一名患有难治性贫血罕见病例的患者,通过G带和连续C带鉴定出其存在源自5号和8号染色体的获得性标记。将该病例与已发表的此类广泛疾病中5号染色体缺失的各种图示进行比较,结果显示,在(骨髓中典型的)条带缺失或不合格的情况下,核型错误分类可能有助于解释5q-标记在大小和形态上的显著差异。