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子宫平滑肌瘤细胞遗传学。III. 核型正常的子宫平滑肌瘤的间期细胞遗传学分析排除了未检测到的12号三体的可能性。

Uterine leiomyoma cytogenetics. III. Interphase cytogenetic analysis of karyotypically normal uterine leiomyoma excludes possibility of undetected trisomy 12.

作者信息

Vanni R, Van Roy N, Lecca U, Speleman F

机构信息

Istituto di Biologia Generale, Università degli Studi, Cagliari, Italy.

出版信息

Cancer Genet Cytogenet. 1992 Aug;62(1):40-2. doi: 10.1016/0165-4608(92)90035-7.

Abstract

Uterine leiomyoma, a benign tumor that histopathologically is rather homogeneous, was recently characterized cytogenetically. About 40% of the investigated tumors are associated with clonal chromosome abnormalities and five different subgroups have been identified, characterized by trisomy 12, t(12;14)(q14-15;q23-24), del(7q), t(1;2)(p36;p24), and 6p rearrangements. In our survey of 76 cases, trisomy 12 was observed in 10% of the abnormal cases. To exclude a possible underscoring of this abnormality, we reexamined 15 of the cases with normal karyotype by interphase cytogenetics using a chromosome 12 alphoid DNA probe.

摘要

子宫平滑肌瘤是一种组织病理学上较为均一的良性肿瘤,最近在细胞遗传学方面得到了表征。约40%的被研究肿瘤与克隆性染色体异常相关,并且已经鉴定出五个不同的亚组,其特征分别为12号染色体三体、t(12;14)(q14 - 15;q23 - 24)、7号染色体长臂缺失、t(1;2)(p36;p24)以及6号染色体短臂重排。在我们对76例病例的调查中,10%的异常病例观察到了12号染色体三体。为排除这种异常可能被低估的情况,我们使用12号染色体α卫星DNA探针,通过间期细胞遗传学对15例核型正常的病例进行了重新检测。

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