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唐氏综合征中额外21号染色体的起源。对26个信息丰富的家族中荧光变体和卫星关联的研究。

The origin of the extra chromosome 21 in Down syndrome. Studies of fluorescent variants and satelite association in 26 informative families.

作者信息

Hansson A, Mikkelsen M

出版信息

Cytogenet Cell Genet. 1978;20(1-6):194-203. doi: 10.1159/000130851.

Abstract

Studies of fluorescence and other chromosomal variants were informative in 26 out of 72 families. Maternal nondisjunction was found in 19 and paternal in 7 cases. Satellite association studies of these parents and 94 controls from the same age group showed a highly significant increase in the satellite association index (AI) for chromosome 21 in the parents where the nondisjunctional event had taken place. The AI was also higher for chromosome 14. In addition, the parents who produced the normal gametes had significantly higher AI's for some acrocentrics than the controls. Exogenous factors increasing satellite association cannot be ruled out. The number of 21-21 association was significantly increased in the parents with nondisjunction in meiosis 1. The results indicate that satellite association may play a role in the etiology of Down syndrome.

摘要

在72个家庭中的26个家庭里,对荧光及其他染色体变异的研究提供了有用信息。发现19例为母源不分离,7例为父源不分离。对这些父母以及来自同一年龄组的94名对照者进行的随体联合研究显示,在发生不分离事件的父母中,21号染色体的随体联合指数(AI)显著升高。14号染色体的AI也更高。此外,产生正常配子的父母某些近端着丝粒染色体的AI明显高于对照者。不能排除增加随体联合的外源性因素。减数分裂Ⅰ期发生不分离的父母中,21-21联合的数量显著增加。结果表明随体联合可能在唐氏综合征的病因学中起作用。

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