Flinter F A, Bobrow M
Paediatric Research Unit, United Medical School, Guy's Hospital, London, UK.
Pediatr Nephrol. 1988 Jul;2(3):343-50. doi: 10.1007/BF00858691.
The rapid development of new techniques in molecular biology is leading to identification of the genes responsible for a wide variety of diseases. Several renal conditions are caused by gene defects and are amenable to this approach. The process of gene mapping is discussed and the current position regarding prenatal diagnosis and carrier testing for genetic renal disease is reviewed.
分子生物学新技术的迅速发展促使人们识别出多种疾病的致病基因。一些肾脏疾病由基因缺陷引起,适合采用这种方法进行研究。本文讨论了基因定位的过程,并综述了目前关于遗传性肾脏疾病的产前诊断和携带者检测的进展情况。