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染色体失衡、正常表型与印记

Chromosome imbalance, normal phenotype, and imprinting.

作者信息

Bortotto L, Piovan E, Furlan R, Rivera H, Zuffardi O

机构信息

Istituto Immunotrasfusionale, Ospedale Civile di Udine, Italy.

出版信息

J Med Genet. 1990 Sep;27(9):582-7. doi: 10.1136/jmg.27.9.582.

Abstract

A duplication of the sub-bands 1q42.11 and 1q42.12 was found in a boy and his mother. The proband has short stature (around the 10th centile) but a normal phenotype and psychomotor development. His mother is also asymptomatic. We found 30 published cases of normal subjects with an imbalance of autosomal euchromatic material. In these cases the imbalance involved either only one G positive band or a G positive and a G negative band. Thus the absence of a phenotypic effect cannot always be ascribed to the deficiency in the G positive bands of coding DNA. Moreover, in some cases, the method of transmission of the chromosome abnormality was such that an imprinting effect could be postulated.

摘要

在一名男孩及其母亲身上发现了1q42.11和1q42.12亚带的重复。先证者身材矮小(约第10百分位),但表型和精神运动发育正常。他的母亲也没有症状。我们发现有30例已发表的正常受试者常染色体常染色质物质失衡的病例。在这些病例中,失衡仅涉及一条G阳性带或一条G阳性带和一条G阴性带。因此,表型效应的缺失不能总是归因于编码DNA的G阳性带的缺乏。此外,在某些情况下,染色体异常的传递方式使得可以假定存在印记效应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eed/1017222/e232eeaabdab/jmedgene00047-0047-a.jpg

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