摘要
血友病的基因诊断是预防血友病患者出生，实现优生优育的根本措施。综合使用直接和间接基因诊断措施是血友病基因诊断的基本策略；在进行间接基因诊断时，应该重视选择基因内位点和多个基因外位点联合提供的信息。
The genetic diagnosis of hemophilia is a basic method for preventing the birth of hemophilia patients and a basic way for realizing the aim of aristogenesis. Direct and indirect genetic diagnosis is a basic strategy for screening of hemophilia ; while in indirect genetic diagnosis, more attention should be paid on the information given by the intro-genetic sites combined with the extra-genetic sites.
出处
《中华检验医学杂志》
CAS
CSCD
北大核心
2008年第1期6-8,共3页
Chinese Journal of Laboratory Medicine
关键词
血友病A
分子诊断技术
倒位
染色体
突变
Hemophilia A
Molecular diagnostic techniques
Inversion, chromosome
Mutation
