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18三体综合征中额外染色体的亲本来源。

Parental origin of the supernumerary chromosome in trisomy 18.

作者信息

Ya-gang X, Robinson W P, Spiegel R, Binkert F, Ruefenacht U, Schinzel A A

机构信息

Institute of Medical Genetics, University of Zürich, Switzerland.

出版信息

Clin Genet. 1993 Aug;44(2):57-61. doi: 10.1111/j.1399-0004.1993.tb03847.x.

Abstract

The parental origin of an extra chromosome in Edwards syndrome has been investigated in 23 families by the combination of the VNTR probe pERT25, two microsatellite polymorphisms for D18S34 and D18S40, and several two-allele polymorphisms. Of the 23 cases, 22 were informative, with 17 (77%) being maternal and 5 (23%) paternal in origin. These results support the previous investigations, suggesting that trisomy 18 is predominantly of maternal origin, although a higher rate of paternally derived cases was observed than previously reported. A significant increase in maternal age was found to be associated with meiotic nondisjunction. Parental age was increased in both the maternally and paternally derived cases, but the size of the latter class was small and did not reach statistical significance.

摘要

通过运用VNTR探针pERT25、D18S34和D18S40的两种微卫星多态性以及几种双等位基因多态性,对23个家庭中爱德华兹综合征额外染色体的亲本来源进行了研究。在这23个病例中,22个具有信息性,其中17个(77%)起源于母亲,5个(23%)起源于父亲。这些结果支持了先前的研究,表明18三体主要起源于母亲,尽管观察到父源病例的发生率高于先前报道。发现母亲年龄的显著增加与减数分裂不分离有关。母源和父源病例的父母年龄均有所增加,但后一类的数量较少,未达到统计学意义。

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