Cooper D N, Jay M, Bhattacharya S, Jay B
Haematology Department, King's College Hospital School of Medicine, Denmark Hill, London.
Eye (Lond). 1987;1 ( Pt 6):699-721. doi: 10.1038/eye.1987.114.
In this review of the recent literature, the contribution that the new techniques of molecular genetics has made in the analysis and diagnosis of human ophthalmic conditions is presented and discussed. Among the disorders reviewed are X-linked retinitis pigmentosa, Norrie's disease, gyrate atrophy and retinoblastoma, and there are also sections on crystallins and visual pigments.
在这篇近期文献综述中,介绍并讨论了分子遗传学新技术在人类眼科疾病分析和诊断中所做的贡献。所综述的疾病包括X连锁视网膜色素变性、诺里病、回旋状萎缩和视网膜母细胞瘤,此外还有关于晶状体蛋白和视觉色素的章节。