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对具有明显平衡结构重排的表型异常患者进行高分辨率染色体分析。

High-resolution chromosome analysis of phenotypically abnormal patients with apparently balanced structural rearrangements.

作者信息

Raimondi S C, Luthardt F W, Summitt R L, Martens P R

出版信息

Hum Genet. 1983;63(4):310-4. doi: 10.1007/BF00274751.

Abstract

Thirteen phenotypically abnormal patients with previously identified de novo or familial, apparently balanced, chromosome rearrangements were reexamined with high-resolution techniques. No definite imbalance could be demonstrated in any of the cases. However, some breakpoints were reassigned to more specific sub-bands and others to totally different bands. The study confirmed translocation reciprocity in some cases in which metaphase banding techniques failed to allow such determination. In one patient an apparent extra dark band was observed which could be explained by limited uncoiling, intraband exchange or small band duplication. In two patients limited uncoiling was observed in one derivative chromosome. Tissue-limited mosaicism was discovered in cultured fibroblasts from one of the seven patients evaluated.

摘要

对13例先前已鉴定出为新发或家族性、明显平衡的染色体重排的表型异常患者,采用高分辨率技术进行了重新检查。在任何病例中均未发现明确的不平衡。然而,一些断点被重新定位到更特定的亚带,另一些则被定位到完全不同的带。该研究证实了在一些中期显带技术无法进行此类判定的病例中存在易位互换性。在一名患者中观察到一条明显多余的暗带,这可以通过有限的解旋、带内交换或小带重复来解释。在两名患者中,在一条衍生染色体上观察到有限的解旋。在评估的7名患者中的1名患者的培养成纤维细胞中发现了组织局限性嵌合体。

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