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Prenatal diagnosis of a de novo trisomy 20p detected by noninvasive prenatal testing
Prenatal diagnosis of trisomy 20p seems to be difficult, considering the capacity of ultrasound to detect mild dysmorphic. NIPT has good performance in detecting fetal trisomy 20p combined with low coverage WGS and karyotype analysis.
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| Veröffentlicht in: | Clin Case Rep |
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| Hauptverfasser: | , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
John Wiley and Sons Inc.
2021
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8077397/ https://ncbi.nlm.nih.gov/pubmed/33936600 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.3587 |
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