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母亲发生(9;18)易位,育有两个异常后代,每个后代具有不同的染色体衍生物。

Maternal translocation (9;18) with two abnormal offspring each with different chromosome derivatives.

作者信息

Pearson M, Riske C, Allanson J E

机构信息

Genetics Center of Southwest Biomedical Research Institute, Scottsdale, Arizona 85251.

出版信息

J Med Genet. 1989 Oct;26(10):655-8. doi: 10.1136/jmg.26.10.655.

Abstract

We report a phenotypically normal woman with an apparently balanced reciprocal translocation between chromosomes 9 and 18 [46,XX,t(9;18)(p22;p11.2)], giving rise to unbalanced chromosome complements in two of her children, each of whom received a different derivative chromosome. The proband's karyotype is 46,XY,-18,+der(18), t(9;18)(p22;p11.2)mat, which results in a duplication of the distal portion of the short arm of chromosome 9 with a concomitant deletion of much of the short arm of chromosome 18. The karyotype of the proband's brother is 46, XY,-9,+der(9),t(9;18)(p22;p11.2)mat, which results in a deletion of the distal short arm of chromosome 9 and a duplication of most of the short arm of chromosome 18. The phenotype of each child is significantly different from that of his sib and is not consistent with any previously reported chromosome abnormality.

摘要

我们报告了一名表型正常的女性,其9号和18号染色体之间存在明显平衡的相互易位[46,XX,t(9;18)(p22;p11.2)],导致她的两个孩子出现染色体组成不平衡,每个孩子都获得了一条不同的衍生染色体。先证者的核型为46,XY,-18,+der(18), t(9;18)(p22;p11.2)mat,这导致9号染色体短臂远端部分重复,同时18号染色体短臂大部分缺失。先证者兄弟的核型为46, XY,-9,+der(9),t(9;18)(p22;p11.2)mat,这导致9号染色体短臂远端缺失,18号染色体短臂大部分重复。每个孩子的表型与其兄弟姐妹的表型显著不同,且与之前报道的任何染色体异常均不一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5987/1015721/8df1cdd46b79/jmedgene00060-0048-a.jpg

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