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Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 42,910 single pregnancies with different clinical features

BACKGROUND: Since the discovery of cell-free DNA (cfDNA) in maternal plasma, it has opened up new approaches for non-invasive prenatal testing. With the development of whole-genome sequencing, small subchromosomal deletions and duplications could be found by NIPT. This study is to review the efficac...

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Detaylı Bibliyografya
Yayımlandı:Hum Genomics
Asıl Yazarlar: Chen, Yibo, Yu, Qi, Mao, Xiongying, Lei, Wei, He, Miaonan, Lu, Wenbo
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2019
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6884830/
https://ncbi.nlm.nih.gov/pubmed/31783780
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40246-019-0250-2
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