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Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype
BACKGROUND: Submicroscopic chromosomal imbalance is associated with an increased nuchal translucency (NT). Most previous research has recommended the use of chromosomal microarray analysis (CMA) for prenatal diagnosis if the NT ≥ 3.5 mm. However, there is no current global consensus on the cutoff va...
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| Yayımlandı: | Mol Genet Genomic Med |
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| Asıl Yazarlar: | , , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
John Wiley and Sons Inc.
2019
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6687862/ https://ncbi.nlm.nih.gov/pubmed/31209990 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.811 |
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