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出 处:《中国优生与遗传杂志》2009年第10期47-48,共2页Chinese Journal of Birth Health & Heredity
摘 要:目的建立一种成功率高,收获分裂相多的羊水细胞培养方法。方法总共83例羊水标本分成两组分别用经典培养法和传代培养法培养。结果经典培养成功率为90.6%(39/43),传代培养成功率为95%(38/40),传代培养方法成功率高于经典培养方法,且所获分裂相数目多,形态好。结论传代培养方法是一种简便易行的羊水细胞培养方法。Objective : The aim of this study is to establish an amniotic fluid cultivation method of high successful rate. Methods : The classic cultivation method was performed in 43 cases of amniotic fluid cultivation and serial subcultivation method was performed in 40 cases of amniotic fluid cultivation. Results : The successful rate of classic cultivation method and serial subcultivation method was 90. 4% (39/43) and 95% (38/40) respectively. The serial subcultivation has high successful rate than the classics culture. More and high - quality M - phase can be observed by serial subcuhivation method. Conclusion: The serial subcuhivation is convenient method in amniotic fluid culture. It has the advantages of good chromosome morphous and high successful rate.
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