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Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal Translucency
We have carried out a retrospective study of chromosome anomalies associated with increased nuchal translucency (NT) in order to compare yield rates of karyotype, chromosome microarray analysis (CMA), and non-invasive prenatal testing (NIPT) in this condition. Presenting with increased NT or cystic...
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| Yayımlandı: | Med Sci (Basel) |
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| Asıl Yazarlar: | , , , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
MDPI
2019
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6473420/ https://ncbi.nlm.nih.gov/pubmed/30818867 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/medsci7030040 |
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