Home /Research /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

Year
2014
Citations
10
Access
Open access

Keywords

Massive parallel sequencingMedicineAneuploidyChromosomeTrisomyCell-free fetal DNAObstetricsFetusGeneticsPrenatal diagnosis

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