Methods: HOXA13 gene was detected in 58 Chinese Han patients(including 51 patients with incomplete Mllerian fusion, 7 congenital absence of uterus and vagina (CAUV)) and 54 control individuals.
方法:对58例中国汉族苗勒管发育异常患者(包括51例苗勒管融合不全患者、7例先天性无阴道无子宫患者)和54例正常对照者进行HOXA13基因检测。
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