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母女均存在X染色体短臂重复。

Duplication of the short arm of the X chromosome in mother and daughter.

作者信息

Tuck-Muller C M, Martinez J E, Batista D A, Kearns W G, Wertelecki W

机构信息

Department of Medical Genetics, University of South Alabama, College of Medicine, Mobile 36688.

出版信息

Hum Genet. 1993 May;91(4):395-400. doi: 10.1007/BF00217366.

Abstract

An 11-year-old girl with short stature, mental retardation, and mild dysmorphic features was found to have an inverted duplication of most of the short arm of the X chromosome [dic inv dup(X)(qter-->p22.3::p22.3-->cen:)]. Her mother, who is also short and retarded, carries the same duplication. Fluorescence in situ hybridization with an X chromosome library, and with X centromere-specific alpha satellite and telomere probes, was useful in characterizing the duplication. In most females with structurally abnormal X chromosomes, the abnormal chromosome is inactivated. Although the duplicated X was consistently late replicating in the mother, X chromosome inactivation studies in the proband indicated that in 11% of her lymphocytes the duplicated X was active.

摘要

一名11岁身材矮小、智力发育迟缓且有轻度畸形特征的女孩被发现X染色体短臂的大部分发生了反向重复[双着丝粒反向重复(X)(qter→p22.3::p22.3→cen:)]。她同样身材矮小且智力发育迟缓的母亲也携带相同的重复。用X染色体文库以及X着丝粒特异性α卫星和端粒探针进行荧光原位杂交,有助于对该重复进行特征分析。在大多数X染色体结构异常的女性中,异常染色体是失活的。尽管母亲体内重复的X染色体始终复制延迟,但对先证者的X染色体失活研究表明,在她11%的淋巴细胞中,重复的X染色体是活跃的。

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