Barker P E, Mohandas T, Kaback M M
Clin Genet. 1977 Apr;11(4):243-8. doi: 10.1111/j.1399-0004.1977.tb01308.x.
Frequencies of 12 fluorescent chromosome polymorphisms were scored from Q-banded karyotypes derived from 108 midtrimester diagnostic amniotic fluid cell cultures. The most frequent variants were the bright fluorescent short arm of chromosome 13 (P = 0.458) and the bright fluorescent marker close to the centromere on chromosome 3 (P = 0.426).The polymorphism pattern was found to be different between the maternal (blood culture) and fetal (amniotic fluid cell culture) karyotypes in each of the 25 paired cases studied. This technique is valuable in prenatal diagnosis to exclude possible maternal cell contamination and outgrowth in cases where the amniotic fluid cell cultures reveal a female karyotype.
从108例孕中期诊断性羊水细胞培养获得的Q带核型中,对12种荧光染色体多态性的频率进行了评分。最常见的变异是13号染色体短臂的明亮荧光(P = 0.458)和3号染色体靠近着丝粒的明亮荧光标记(P = 0.426)。在所研究的25对病例中,每一对病例的母体(血培养)和胎儿(羊水细胞培养)核型的多态性模式均不同。在羊水细胞培养显示为女性核型的病例中,该技术对于排除可能的母体细胞污染和生长在产前诊断中具有重要价值。