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性染色体单体的细胞遗传学和分子分析

Cytogenetic and molecular analysis of sex-chromosome monosomy.

作者信息

Hassold T, Benham F, Leppert M

机构信息

Department of Pediatrics, Cornell University Medical College, New York.

出版信息

Am J Hum Genet. 1988 Apr;42(4):534-41.

Abstract

X chromosome- and Y chromosome-specific DNA probes were used to study different aspects of the genesis of sex-chromosome monosomy. Using X-linked RFLPs, we studied the parental origin of the single X chromosome in 35 spontaneously aborted and five live-born 45,X conceptions. We determined the origin in 35 cases; 28 had a maternal X (Xm) and seven had a paternal X (Xp). There was a correlation between parental origin and parental age, with the Xp category having a significantly reduced mean maternal age by comparison with the Xm group. Studies aimed at detecting mosaicism demonstrated the presence of a Y chromosome or a second X chromosome in three of 33 spontaneous abortions, a level of mosaicism much lower than that reported for live-born Turner syndrome individuals.

摘要

使用X染色体和Y染色体特异性DNA探针来研究性染色体单体发生的不同方面。利用X连锁限制性片段长度多态性(RFLPs),我们研究了35例自然流产和5例活产的45,X胚胎中单一X染色体的亲本来源。我们确定了35例的来源;28例有一条母源X染色体(Xm),7例有一条父源X染色体(Xp)。亲本来源与亲本年龄之间存在相关性,与Xm组相比,Xp组的平均母龄显著降低。旨在检测嵌合体的研究表明,33例自然流产中有3例存在Y染色体或第二条X染色体,嵌合水平远低于活产特纳综合征患者的报道水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1029/1715233/01e7beadb2e9/ajhg00127-0015-a.jpg

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