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唐氏综合征筛查研究进展 被引量:10

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摘要 一、唐氏综合征的概述唐氏综合征或称21-三体综合征是人类生后常见的常染色体异常疾病,也是智力低下的最常见病因,发病率约为1/800~1/600,高龄产妇的发病率较高,主要的发病机制是卵母细胞减数分裂不分离,95%的病人受精卵中21号染色体额外复制,
出处 《中国优生与遗传杂志》 2012年第7期4-6,3,共4页 Chinese Journal of Birth Health & Heredity
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同被引文献65

  • 1龙峰,段纯,刘佳南,廖旭东,林冰英.孕中期甲胎蛋白异质体在唐氏综合征筛查中的临床意义[J].中国医学前沿杂志(电子版),2014,6(3):43-45. 被引量:5
  • 2王丹,刘丽,宋朝晖,董佳.3657例孕中期唐氏筛查及产前诊断的临床价值分析[J].中国产前诊断杂志(电子版),2010,2(3):17-20. 被引量:17
  • 3侯红瑛,李小毛,滕奔琦,尹玉竹,许成芳,易翠兴.妊娠中晚期羊水细胞核型分析[J].中国优生与遗传杂志,2006,14(8):42-44. 被引量:34
  • 4朱俊真,余小平,张德峰,郭文潮.唐氏综合征儿出生和母龄年轻化变动趋势及预防策略[J].中国优生与遗传杂志,2006,14(11):49-49. 被引量:20
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