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甲型血友病是凝血因子Ⅷ（ＦⅧ）基因缺陷导致的一种遗传性出血性疾病。近年来已发现大量甲型血友病的基因缺陷。我们应用聚合酶链反应（ＰＣＲ）技术，分析了云南省傣、彝、汉族人ＳＴ１４（ＤＸＳ５２）可变数目串联重复序列（ＶＮＴＲ）的多态性特点，现报道如下。对象...
Hemophilia A is a hereditary hemorrhagic disease caused by a deficiency of Factor VIII (FⅧ) gene. In recent years, a large number of genetic defects in hemophilia A have been found. Using polymerase chain reaction (PCR), we analyzed the polymorphism of variable number tandem repeat (VNTR) of ST14 (DXS52) in Dai, Yi and Han nationalities in Yunnan Province, and are reported as follows. Object ...