Mouse autosomal trisomy - two's company, three's a crowd

被引:40
作者
Hernandez, D [1 ]
Fisher, EMC [1 ]
机构
[1] St Marys Hosp, Imperial Coll, Sch Med, Dept Neurogenet, London W2 1PG, England
基金
英国惠康基金;
关键词
D O I
10.1016/S0168-9525(99)01743-6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Autosomal trisomy causes a large proportion of all human pregnancy loss and so is a significant source of lethality in the human population, The autosomal trisomy syndromes each have a different phenotype and are probably caused by the effects of specific genes that are present in three copies, rather than the normal two. Identifying these genes will require the application of classical genetic and new genome-manipulation approaches. Recent advances in chromosome engineering are now allowing us to create precisely defined autosomal trisomies in the mouse, and so provide new routes to identifying the critical, dosage-sensitive genes that are responsible for these highly deleterious, yet very common, syndromes.
引用
收藏
页码:241 / 247
页数:7
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