用α珠蛋白基因探针和DNA印迹杂交法对17例有血红蛋白H病高风险胎儿进行了产前基因诊断,诊断结果有5例为α地中海贫血(α地贫)1杂合子或正常,5例为α地贫2杂合子,3例为血红蛋白H病,1例为血红蛋白Bart胎儿水肿综合征,其余3例由于双亲一方为非缺失型α地贫,故对其胎儿的基因型不能作出准确诊断。
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