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因新发(6号染色体短臂;13号染色体长臂)易位导致的13号染色体部分三体。

Partial trisomy 13 as a result of de novo (6p;13q) translocation.

作者信息

Jones L A, Taysi K, Strauss A W, Hartmann A F

出版信息

Hum Genet. 1979 Apr 27;48(2):245-9. doi: 10.1007/BF00286911.

Abstract

A newborn infant with the clinical features of the Patau syndrome was found to have excess chromosome 13 material present as a tandem translocation involving the short arm of chromosome 6 and the long arm of an extra chromosome 13: 46,XY,t(6;13)(p24;q12). The major part of the long arm of the extra chromosome 13 was attached linearly (tandem translocation) to the short arm of chromosome 6. Both parents were phenotypically and karyotypically normal.

摘要

一名具有帕陶氏综合征临床特征的新生儿被发现有额外的13号染色体物质,表现为涉及6号染色体短臂和一条额外13号染色体长臂的串联易位:46,XY,t(6;13)(p24;q12)。额外13号染色体长臂的主要部分线性连接(串联易位)到6号染色体短臂上。父母双方在表型和核型上均正常。

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