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11-13周胎儿非整倍体染色体的筛查 被引量:1

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摘要 应该在孕早期对胎儿非整倍体染色体疾病进行有效地筛查。目前,通过测量颈透明层(NT)厚度及测定孕妇血清游离β-HCG和PAPP-A浓度可检出90%的21-三体及其它非整倍体患儿,其筛查阳性率为5%。
出处 《中国优生与遗传杂志》 2012年第8期9-10,3,共3页 Chinese Journal of Birth Health & Heredity
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