Ferti A, Tsikritzi H, Yialamboukides M, Economopoulos T, Panani A, Lyberatos C
5th Medical Department, Evangelismos Hospital, Athens, Greece.
Cancer Genet Cytogenet. 1992 Feb;58(2):201-3. doi: 10.1016/0165-4608(92)90114-n.
In a case with splenomegaly of unknown origin and features of hypersplenism, an interstitial 9q deletion was identified as a sole clonal abnormality of bone marrow cells. The meaning of 9q deletion as a primary change, as well as its clinical significance, are considered.
在一例病因不明的脾肿大并伴有脾功能亢进特征的病例中，间质9q缺失被确定为骨髓细胞唯一的克隆性异常。本文对9q缺失作为原发性改变的意义及其临床意义进行了探讨。
