首页 /研究 /Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA
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Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA

Francesca Romana Grati, José Carlos Ferreira, Komal Bajaj

发表年份
2014
引用次数
10
访问权限
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关键词

Massive parallel sequencingMedicineAneuploidyChromosomeTrisomyCell-free fetal DNAObstetricsFetusGeneticsPrenatal diagnosis

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