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由t(10;21)易位导致的家族性唐氏综合征:唐氏表型与21号染色体特定片段三体性相关的证据。

Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment of chromosome 21.

作者信息

Williams J D, Summitt R L, Martens P R, Kimbrell R A

出版信息

Am J Hum Genet. 1975 Jul;27(4):478-85.

Abstract

This report deals with a reciprocal t(10;21) translocation which is observed in three generations of a family. Included are examples of the balanced translocation, adjacent-2 segregation producing three patients with trisomy of the distal long arm of chromosome 21 and the Down syndrome, and 3-1 disjunction producing trisomy of the proximal segment of chromosome 21 in a mildly mentally retarded boy without phenotypic features of the Down syndrome. These data provide evidence that the Down phenotype is attributable to trisomy of the distal long arm of chromosome 21.

摘要

本报告涉及一个在一个家族三代人中均观察到的相互易位t(10;21)。其中包括平衡易位的例子、产生三名21号染色体长臂远端三体患者及唐氏综合征的邻接-2分离,以及在一名无唐氏综合征表型特征的轻度智力发育迟缓男孩中产生21号染色体近端三体的3-1分离。这些数据提供了证据,表明唐氏综合征表型归因于21号染色体长臂远端三体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3f1/1762808/044e5ba09912/ajhg00437-0041-a.jpg

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