Wieacker P, Müller C R, Siebers J W
J Perinat Med. 1986;14(2):127-30. doi: 10.1515/jpme.1986.14.2.127.
A cloned DNA fragment from a Y chromosome genomic library was used for prenatal sex determination. Native cells from as little as 0.5 ml of amniotic fluid were analyzed by a dot blot hybridization technique without prior cell culture. Identification of male fetuses was possible within 3 days and confirmed by subsequent conventional karyotyping. This method of rapid sex screening is an alternative to the other methods of prenatal determination to the conventional chromosome analysis because it is a more rapid method, and to the karyotyping of chorion biopsy material because amniocentesis seems to have a lower risk and can still be performed when chorion biopsy is not more possible.
来自Y染色体基因组文库的一个克隆DNA片段被用于产前性别鉴定。通过斑点印迹杂交技术对仅0.5毫升羊水的原始细胞进行分析,无需事先进行细胞培养。在3天内即可鉴定出男性胎儿,并通过后续的传统核型分析加以确认。这种快速性别筛查方法是产前性别鉴定的其他方法的一种替代方案,它相对于传统染色体分析而言是一种更快的方法,相对于绒毛取样材料的核型分析而言,因为羊膜穿刺术似乎风险更低,并且在无法进行绒毛取样时仍可进行。